Optically active 1-phenyl-2-substituted propane derivatives and methods of producing the same

ABSTRACT

An (S)-1-phenyl-2-substituted propane derivative shown by the following formula (I) ##STR1## wherein R 1  and R 2  represent a lower alkyl group, etc., or R 1  and R 2  may form together an alkylene group, etc.; R 3 , R 4  and R 5  represent a hydrogen atom, etc.; and X represents a hydroxyl group which may be protected with a protective group, or a halogen atom etc., can readily be produced (i) by permitting a microorganism belonging to the genus Torulaspora, the genus Candida, the genus Pichia or the like to act on a phenylacetone derivative and asymmetrically reducing the compound, or (ii) by sterically inverting an (R)-enantiomer. (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative having a high optical purity can easily be obtained from the compound of the formula (I). The ethanol derivative is useful as an anti-obesity agent and the like.

This is a division of application Ser. No. 08/613,946, filed Mar. 13, 1996, now U.S. Pat. No. 5,679,557.

FIELD OF THE INVENTION

The present invention relates to an optically active (S)- or (R)-1-phenyl-2-substituted propane derivative which is an important intermediate for synthesis of an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative, and a method of producing the same. The present invention further relates to a method of producing the ethanol derivative which is useful as a medical compound or an intermediate product thereof.

BACKGROUND OF THE INVENTION

As anti-obesity agents or anti-diabetic agents belonging to a new category of agents without using insulin, 1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivatives are noted since the derivatives act selectively on a β₃ -receptor in vivo, thus having extremely low side effects. Pharmacological studies on the 1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivatives have revealed that the β₃ -action substantially depends on (R,R)-enantiomers thereof (see J. Med. Chem., 35, 3081 (1992), and U.S. Pat. No. 5,061,727). For example, the above-mentioned U.S. Patent discloses that an (R,R)-5- 2- 2-(3-chlorophenyl)-2-hydroxyethyl!amino!propyl!-1,3-benzodioxole-2,2-dicarboxylic acid disodium salt has a higher activity than the corresponding (S,S)-enantiomer by a factor of 47.

For the production of an optically active 1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative, there is known an optical resolution of a racemic form or a racemate, or an asymmetric synthesis.

For example, the above mentioned U.S. Pat. No. 5,061,727 discloses a method of producing an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative which comprises (1) allowing a racemic 2-amino-1-phenylethanol derivative to react with a phenylacetone derivative and sodium cyanoborohydride to produce a mixture of four species of optical isomers of a 1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative, (2) isolating and removing an (R,S)-isomer and an (S,R)-isomer from the mixture, and (3) optically resoluting an (R,R)-isomer and an (S,S)-isomer by a diastereomer method. According to this method, however, it is necessary to isolate and purify only the (R,R)-isomer from the mixture of the four species of optical isomers, therefore, the processes are complicated and the yield is decreased. Further, since large quantities of raw materials are required, the method is also disadvantageous in economical factor.

The U.S. Patent and the Journal of Medicinal Chemistry as mentioned above disclose a method allowing an (R)-3-chlorostyrene oxide derivative to react with an (R)-1-methyl-2-phenylethylamine derivative. The (R)-1-methyl-2-phenylethylamine derivative used as a raw material or reactant in the method, however, has a strong antihypnotic or arousal action and it requires a particular attention when handled, therefore is not suited for a use in commercial production. Further, a lot of steps or processes are required to obtain the above-mentioned two reactants. For instance, the (R)-3-chlorostyrene oxide derivative is prepared from an acetophenone derivative through three steps, that is, chlorination, asymmetric reduction and epoxidation, and the (R)-1-methyl-2-phenylethylamine derivative is prepared from L-DOPA through six steps, namely, introduction of a protective group into an amino group, esterification, reduction of the resulting ester, converting a hydroxyl group to a mesyloxy group, removal of the protective group and reduction.

SUMMARY OF THE INVENTION

Accordingly, it is an object of the present invention to provide an optically active compound which is useful for the efficient production of an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative with a good yield.

It is another object of the invention to provide a process for producing the compound efficiently with high yield and optical purity.

Still another object of the invention is to provide an optically active compound which is useful for the production of the derivative and is available and easy to handle or treat.

It is a further object of the present invention to provide a process for producing an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative having a higher optical purity efficiently with a high yield.

A yet further object of the present invention is to provide an optically active (R)-enantiomer which is suitable for the production of the optically active compound being useful for producing the (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative, and a process for producing the same.

The present invention further relates to a process for asymmetrically reducing an phenylacetone derivative to the optically active compound, and to a use of a microorganism in production of the optically active intermediate.

After much studies and efforts to accomplish the above mentioned objects, the present inventors found that an optically active (S)- or (R)-1-phenyl-2-substituted propane derivative having a high optical purity can be obtained with a high yield by permitting a microorganism capable of asymmetrically reducing a phenylacetone derivative to act on the phenylacetone derivative, and that an optically active (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative can easily or readily be produced from the (S)- or (R)-1-phenyl-2-substituted propane derivative with high yield and selectivity. The present invention has been accomplished based on the above findings.

Thus, the present invention provides an (S)-1-phenyl-2-substituted propane derivative shown by the following formula (I) ##STR2## wherein R¹ and R² represent (a) the same or different, a hydrogen atom or a protective group for hydroxyl group, or (b) R¹ and R² may form an optionally substituted ring with the adjacent oxygen atoms; R³, R⁴ and R⁵ independently represent a hydrogen atom, a lower alkyl group, a lower haloalkyl group, a lower alkoxy group, a nitro group or a halogen atom; and X represent a hydroxyl group which may be protected with a protective group, an optionally substituted alkylsulfonyloxy group, an optionally substituted arylsulfonyloxy group or a halogen atom.

The (S)-1-phenyl-2-substituted propane derivative of the general formula (I) may be produced by, for example, a process which comprises:

permitting a microorganism which is capable of asymmetrically reducing a phenylacetone derivative shown by the following formula (II) ##STR3## wherein R¹, R², R³, R⁴ and R⁵ have the same meanings as defined above, to a corresponding (S)-1-phenyl-2-propanol derivative shown by the following formula (III) ##STR4## wherein R¹, R², R³, R⁴ and R⁵ have the same meanings as defined above, or a preparation thereof

to act on the phenylacetone derivative, and

harvesting or recovering the product (S)-1-phenyl-2-propanol derivative.

Further, the (S)-1-phenyl-2-substituted propane derivative of the general formula (I) may also be obtained by, for instance, allowing a sulfonylating agent or a halogenating agent to react with the (S)-1-phenyl-2-propanol derivative of the general formula (III).

The (S)-1-phenyl-2-substituted propane derivative of the general formula (I) is useful for production of an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative shown by the following formula VI ##STR5## wherein R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and Z have the same meanings as defined above, or a salt thereof.

The present invention further provides an (R)-1-phenyl-2-substituted propane derivative shown by the general formula (VII) ##STR6## wherein R¹, R², R³, R⁴, R⁵ and X have the same meanings as defined above.

The (R)-1-phenyl-2-substituted propane derivative of the general formula (VII) may be produced by, for instance, utilizing a function of a microorganism which is capable of asymmetrically reducing the phenylacetone derivative of the general formula (II) to produce the corresponding (R)-1-phenyl-2-propanol derivative shown by the following formula (VII') ##STR7## wherein R¹, R², R³, R⁴ and R⁵ have the same meanings as defined above, or a preparation thereof.

The (R)-1-phenyl-2-substituted propane derivative of the general formula (VII) may, for instance, be sterically inverted to the (S)-1-phenyl-2-substituted propane derivative of the general formula (I) with the use of a nucleophilic reagent.

The present invention still further discloses a process for asymmetrically reducing the phenylacetone derivative of the general formula (II) to the corresponding (S)- or (R)-1-phenyl propane derivative, and a use of a microorganism capable of asymmetrically reducing the phenylacetone derivative of the general formula (II), or a preparation thereof for the production of the corresponding (S)- or (R)-1-phenyl-2-substituted propane derivative.

DETAILED DESCRIPTION OF THE INVENTION

The (S)-1-phenyl-2-substituted propane derivatives shown by the general formula (I) are particularly useful as intermediates for synthesis of the (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivatives which are usable as medicinal compounds or drugs, or intermediate materials thereof.

As the protective group for hydroxyl group in R¹ and R², there may be mentioned protective groups for a hydroxyl group generally employed in the field of organic synthesis. Such protective groups include, for example, (A) a group which forms an ether bond with an oxygen atom, (B) a group which forms an ester bond with an oxygen atom, (C) a group which forms a carbonate with an oxygen atom and (D) a group which forms a sulfonic acid ester with an oxygen atom.

Examples of the group (A) which forms an ether bond with an oxygen atom include (1) an optionally substituted lower alkyl group, (2) an optionally substituted allyl group, (3) an optionally substituted cycloalkyl group, (4) an optionally substituted heterocyclic group, (5) an optionally substituted aralkyl group and (6) an optionally substituted silyl group.

The optionally substituted lower alkyl group (1) includes, for example, (a) an optionally substituted alkyl group having 1 to 4 carbon atoms such as methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl and t-butyl groups. The substituents for the C₁₋₄ alkyl group include, for example, a C₁₋₄ alkoxy group, a C₁₋₄ alkoxy-C₁₋₄ alkoxy group, a C₇₋₂₀ aralkyloxy group, a benzoyl group, a C₁₋₄ alkylthio group and a halogen atom and so on. Examples of such substituted C₁₋₄ alkyl group include (b) a C₁₋₄ alkoxy-C₁₋₄ alkyl group such as methoxymethyl, ethoxymethyl, t-butoxymethyl, 1-methoxyethyl, 1-ethoxyethyl, 2-methoxyethyl (especially a C₁₋₄ alkoxy-C₁₋₂ alkyl group); (c) an C₁₋₄ alkoxy-C₁₋₄ alkoxy-C₁₋₄ alkyl group such as 2-methoxyethoxymethyl, 2-ethoxymethoxymethyl and the like (specifically a C₁₋₄ alkoxy-C₁₋₄ alkoxy-C₁₋₂ alkyl group); (d) a C₇₋₂₀ aralkyloxy-C₁₋₄ alkyl group such as benzyloxymethyl (especially, a C₇₋₂₀ aralkyloxymethyl group); (e) a phenacyl group; (f) a C₁₋₄ alkylthio-C₁₋₄ alkyl group such as methylthiomethyl, ethylthiomethyl (specifically a C₁₋₄ alkylthiomethyl group); and (g) a C₁₋₄ haloalkyl group having one or more of halogen atoms such as trichloromethyl, trifluoromethyl, 2,2,2-trichloroethyl, 2,2,2-trifluoroethyl and the like.

The optionally substituted allyl group (2) includes, for instance, an allyl group. Examples of the optionally substituted cycloalkyl group (3) include a cycloalkyl group having 3 to 10 carbon atoms such as cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl and cyclodecyl.

As the optionally substituted heterocyclic group (4), there may be mentioned, for example, an optionally substituted 5- to 6-membered heterocyclic group having an oxygen atom or a sulfur atom as a hetero atom. The optionally substituted heterocyclic group may frequently be a perhydroheterocyclic group. The 5- to 6-membered heterocyclic group includes, for instance, tetrahydrofuranyl, tetrahydrothiofuranyl, tetrahydropyranyl and tetrahydrothiopyranyl. Examples of the sustituent for the heterocyclic group include a halogen atom, a C₁₋₄ alkyl group, a C₁₋₄ alkoxy group such as methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, s-butoxy and t-butoxy, and others as mentioned above. Practical examples of the optionally substituted heterocyclic group include an optionally substituted tetrahydropyranyl group (e.g. tetrahydropyranyl, 3-bromotetrahydropyranyl, 4-methoxytetrahydropyranyl, etc.), an optionally substituted tetrahydrothiopyranyl group (for example, tetrahydrothiopyranyl, 3-bromotetrahydrothiopyranyl, 4-methoxytetrahydrothiopyranyl, etc.), an optionally substituted tetrahydrofuranyl group (for instance, tetrahydrofuranyl, etc.), and an optionally substituted tetrahydrothiofuranyl group (e.g. tetrahydrothiofuranyl).

Examples of the optionally substituted aralkyl group (5) include an optionally substituted aralkyl group having 7 to 20 carbon atoms (e.g. benzyl, etc.). The substituent for the aralkyl group includes, for instance, a C₁₋₄ alkyl group; a halogen atom; a nitro group; a C₁₋₄ alkoxy group; a C₆₋₁₂ aryl group such as phenyl. Examples of such substituent may be referred to those in above group (4). Typical examples of the optionally substituted aralkyl group include an optionally substituted C₇₋₂₀ aralkyl group such as benzyl, o-chlorobenzyl, o-nitrobenzyl, p-chlorobenzyl, p-methoxybenzyl, p-methylbenzyl, p-nitrobenzyl, 2,6-dichlorobenzyl, diphenylmethyl, trityl and the like.

The substituent for the silyl group (6) includes a C₇₋₂₀ aralkyl group such as benzyl group and substituents as mentioned in the aralkyl group (5). Examples of the optionally substituted silyl group (6) include trimethylsilyl, triethylsilyl, t-butyldimethylsilyl, tribenzylsilyl, triphenylsilyl and so on.

As the group (B) which forms an ester bond with an oxygen atom, there may be mentioned, for example, an optionally substituted acyl group including (1) an optionally substituted acyl group having 1 to 6 carbon atoms such as formyl, acetyl, chloroacetyl, trifluoroacetyl, propionyl, isopropionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl and the like; (2) an optionally substituted C₇₋₁₆ acyl group having an aromatic ring such as benzoyl, p-phenylbenzoyl, toluoyl, naphthoyl and others; (3) an optionally substituted acyl group having a heterocyclic ring such as furoyl, thenoyl, nicotinoyl and isonicotinoyl groups.

The group (C) which forms a carbonate with an oxygen atom includes, for instance, (1) an optionally substituted C₂₋₅ alkoxycarbonyl group such as methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl, s-butoxycarbonyl and t-butoxycarbonyl; (2) an optionally substituted C₈₋₂₀ aralkyloxycarbonyl group such as benzyloxycarbonyl, p-methoxybenzyloxycarbonyl, p-methylbenzyloxycarbonyl, p-chlorobenzyloxycarbonyl, o-nitrobenzyloxycarbonyl, etc.; (3) an optionally substituted C₇₋₂₀ aryloxycarbonyl group such as phenoxycarbonyl, 4-methylphenyloxycarbonyl, 4-nitrophenyloxycarbonyl, 4-chlorophenyloxycarbonyl, naphthyloxycarbonyl and so on.

Examples of the group (D) which forms a sulfonic acid ester with an oxygen atom include (1) an optionally substituted alkylsulfonyl group such as an optionally substituted C₁₋₄ alkylsulfonyl group (e.g. methanesulfonyl, ethanesulfonyl, trichloromethanesulfonyl, trifluoromethanesulfonyl, etc.); (2) an optionally substituted arylsulfonyl group including an optionally substituted C₆₋₂₀ arylsulfonyl group such as benzenesulfonyl, m-nitrobenzenesulfonyl, p-nitrobenzenesulfonyl, p-chlorobenzenesulfonyl, p-bromobenzenesulfonyl, p-toluenesulfonyl, naphthalenesulfonyl and others.

Preferred examples of R¹ and R² exemplified above include (i) a hydrogen atom; (ii) among the protective groups for hydroxyl group, (A) a group which forms an ether bond with an oxygen atom, specifically, an optionally substituted C₁₋₄ alkyl group and an optionally substituted C₇₋₂₀ aralkyl group, and more specifically a C₁₋₄ alkyl group, and (B) a group which forms an ester bond with an oxygen atom, especially a C₁₋₆ acyl group (e.g. acetyl, etc.).

Where R¹ and R², in incorporation, form a ring together with the adjacent oxygen atoms, the ring may for example be a 5- to 10-membered ring, preferably a 5- to 8-membered ring and more preferably a 5- or 6-membered ring. Such R¹ and R² includes, for instance, an optionally substituted alkylene group, a carbonyl group, a thiocarbonyl group and others.

As the alkylene group, there may be mentioned, for instance, an alkylene group having 1 to 4 carbon atoms such as methylene, ethylene, trimethylene and the like. Preferred alkylene group includes a methylene group.

The optionally substituted methylene group includes, for example, a group shown by the following formula (IX) ##STR8## wherein R^(a) and R^(b) represent, (i) the same or different, a hydrogen atom, a C₁₋₄ alkyl group, a C₁₋₄ haloalkyl group, an optionally substituted C₆₋₂₀ aryl group, a C₁₋₄ alkoxy group, an optionally substituted amino group, a carboxyl group or a salt thereof, an optionally substituted alkoxycarbonyl group, a hydroxymethyl group or an optionally substituted alkoxymethyl group, or (ii) R^(a) and R^(b) may form a C₅₋₇ cycloalkyl group together with the adjacent carbon atom.

The C₁₋₄ alkyl group, the C₁₋₄ haloalkyl group and the C₁₋₄ alkoxy group in R^(a) and R^(b) include those exemplified in R¹ and R². The optionally substituted C₆₋₂₀ aryl group in R^(a) and R^(b) includes, for instance, phenyl, 4-methoxyphenyl, 2-nitrophenyl and others. As the substituted amino group, there may be mentioned, for example, a mono- or di-C₁₋₄ alkylamino group such as methylamino, dimethylamino, ethylamino, diethylamino and others.

As the salt of the carboxyl group represented by R^(a) and R^(b), any salt can be employed. A salt which is pharmacologically acceptable may frequently be used. Examples of such salt include a salt with an inorganic base such as an alkali metal salt (e.g. a sodium salt or a potassium salt), an alkaline earth metal salt (for instance, a magnesium salt, a calcium salt or a barium salt), a metal salt (e.g. a zinc salt or an aluminum salt) and an ammonium salt; a salt with an organic base such as a salt with pyridine, a tri-C₁₋₃ alkylamine (e.g. trimethylamine, triethylamine, etc.) and so on.

The optionally substituted alkoxycarbonyl group in R^(a) and R^(b) includes, for instance, an optionally substituted C₂₋₅ alkoxycarbonyl group as mentioned in R¹ and R².

As examples of the optionally substituted alkoxymethyl group in R^(a) and R^(b), there may be mentioned an optionally substituted a C₁₋₄ alkoxy-methyl group which may be substituted on the alkyl with a substituent. Such substituent for the alkoxymethyl group include, for example, a carboxyl group, a C₂₋₅ alkoxycarbonyl group, a hydroxyl group and a C₁₋₄ alkoxy group. The C₂₋₅ alkoxycarbonyl group and the C₁₋₄ alkoxy group can be referred to the groups as mentioned in R¹ and R². Typical examples of the optionally substituted alkoxymethyl group include (a) a C₁₋₄ alkoxy-methyl group such as methoxymethyl, ethoxymethyl, propoxymethyl, isopropoxymethyl, butoxyemthyl, isobutoxymethyl, s-butoxymethyl and t-butoxymethyl; (b) a carboxy-C₁₋₄ alkoxy-methyl group such as carboxymethoxymethyl, carboxyethoxymethyl, carboxypropoxymethyl, carboxybutoxymethyl, etc.; (c) a C₂₋₅ alkoxycarbonyl-C₁₋₄ alkoxy-methyl group such as methoxycarbonylmethoxymethyl, ethoxycarbonylmethoxymethyl, isopropoxycarbonylmethoxymethyl, 2-butoxycarbonylethoxymethyl and others; (d) a hydroxy-C₁₋₄ alkoxy-methyl group such as 2-hydroxyethoxymethyl, 3-hydroxypropoxymethyl and the like; (e) a C₁₋₄ alkoxy-C₁₋₄ alkoxy-methyl group such as 2-methoxyethoxymethyl, 2-ethoxyethoxymethyl, 3-methoxypropoxymethyl and so on.

The C₅₋₇ cycloalkyl group includes cyclopentyl, cyclohexyl and cycloheptyl groups.

As preferred examples of the optionally substituted methylene group shown by the formula (IX), there may be mentioned, for instance, (a) the group of the formula (IX) wherein R^(a) and R^(b) are, the same or different, a hydrogen atom, a C₁₋₄ alkyl group or a C₅₋₇ cycloalkyl group formed with R^(a), R^(b) and the adjacent carbon atom (e.g. a methylene group, a C₂₋₄ alkylidene group such as an ethylidene group and an isopropylidene group; a C₅₋₇ cycloalkylidene group such as a cyclopentylidene and a cyclohexylidene, and so on); (b) the group of the formula (IX) where R^(a) and R^(b) are respectively a carboxyl group or a salt thereof, an optionally substituted alkoxycarbonyl group, a hydroxymethyl group or an optionally substituted alkoxymethyl group. Specifically preferred is the group of the formula (IX) where R^(a) and R^(b) are, the same or different, a carboxyl group or a salt thereof, or a C₂₋₅ alkoxycarbonyl group.

Practically preferred examples of R¹ and R² include, a hydrogen atom, a C₁₋₄ alkyl group (particularly a methyl group), the optionally substituted methylene group of the formula (IX) formed by incorporation of R¹ and R² where R^(a) and R^(b) are respectively a carboxyl group or a salt thereof, or a C₂₋₅ alkoxycarbonyl group.

Examples of the lower alkyl group in R³, R⁴ and R⁵ include a C₁₋₄ alkyl group as exemplified in R¹ and R².

The lower haloalkyl group in R³, R⁴ and R⁵ includes, for instance, a haloalkyl group having 1 to 4 carbon atoms and one or more of halogen atoms such as chloromethyl, 2-chloroethyl, 4-chlorobutyl, trichloromethyl, trifluoromethyl and 1,1,2,2,2-pentafluoroethyl groups. As examples of the lower alkoxy group and the halogen atom, there may be mentioned a C₁₋₄ alkoxy group and halogen atoms as mentioned in the explanation of R¹ and R².

Preferred substituents of R³, R⁴ and R⁵ include, for example, a hydrogen atom and a lower alkyl group, especially a hydrogen atom.

The protective group of hydroxyl group in X as mentioned above includes an protective group for an alcoholic hydroxyl group usually or generally used in the field of organic synthesis. Examples of such protective group include the protective groups (A) to (C) as mentioned in the protective groups for a hydroxyl group in R¹ and R².

The halogen atom in X includes the halogen atoms mentioned above.

Examples of the optionally substituted alkylsulfonyloxy group in X include an optionally substituted C₁₋₄ alkylsulfonyloxy group such as methanesulfonyloxy, ethanesulfonyloxy, trichloromethanesulfonyloxy and trifluoromethanesulfonyloxy groups.

As examples of the optionally substituted arylsulfonyloxy group, there may be mentioned an optionally substituted C₆₋₂₀ arylsulfonyloxy group such as benzensulfonyloxy, m-nitrobenzenesulfonyloxy, p-nitrobenzenesulfonyloxy, p-chlorobenzenesulfonyloxy, p-bromobenzenesulfonyloxy, p-toluenesulfonyloxy, naphthalenesulfonyloxy and others.

Typical examples of X include a hydroxyl group and a group which plays as a leaving group in a replacement reaction such as an optionally substituted C₁₋₄ alkylsulfonyloxy group, an optionally substituted C₆₋₂₀ arylsulfonyloxy group, a halogen atom and the like. Particularly, a hydroxyl group; an optionally substituted alkylsulfonyloxy group having 1 or 2 carbon atoms such as methanesulfonyloxy group; an optionally substituted arylsulfonyloxy group having 6 to 15 carbon atoms such as p-toluenesulfonyloxy group; chlorine atom, bromine atom and iodine atom are preferable.

In the (S)-1-phenyl-2-substituted propane derivative of the general formula (I), preferred examples include compounds where R¹ and R² are, the same or different, (i) a hydrogen atom, a C₁₋₄ alkyl group (specifically a methyl group) or (ii) R¹ and R² incorporatively form an optionally substituted methylene group of the formula (IX) wherein R^(a) and R^(b) are respectively a carboxyl group or a salt thereof, or a C₂₋₅ alkoxycarbonyl group; R³, R⁴, and R⁵ are independently a hydrogen atom or a C₁₋₄ alkyl group; and X is a hydroxyl group, a C₁₋₂ alkylsulfonyloxy group, a C₆₋₁₅ arylsulfonyloxy group or a halogen atom.

Practical examples of the (S)-1-phenyl-2-substituted propane derivative shown by the general formula (I) include (1) an (S)-1-(3,4-dihydroxyphenyl)-2-substituted propane derivative, (2) an (S)-1-(3,4-di-C₁₋₄ alkoxyphenyl)-2-substituted propane derivative, (3) an (S)-1-(2,2-di-C₁₋₄ alkyl-1,3-benzodioxol-5-yl)-2-substituted propane derivative, (4) an (S)-1- 2,2-bis(C₂₋₅ alkoxycarbonyl)-1,3-benzodioxol-5-yl!-2-substituted propane derivative and (5) an (S)-1-(2,2-dicarboxy-1,3-benzodioxol-5-yl)-2-substituted propane derivative.

As the (S)-1-(3,4-dihydroxyphenyl)-2-substituted propane derivative (1), there may be mentioned, for instance, (S)-1-(3,4-dihydroxyphenyl)-2-propanol, (S)- 2-(3,4-dihydroxyphenyl)-1-methylethyl p-toluenesulfonate!, (S)- 2-(3,4-dihydroxyphenyl)-1-methylethyl methanesulfonate!, (S)-2-chloro-1-(3,4-dihydroxyphenyl)propane, (S)-2-bromo-1-(3,4-dihydroxyphenyl)propane and the like.

Examples of the (S)-1-(3,4-di-C₁₋₄ alkoxyphenyl)-2-substituted propane derivative (2) include (S)-1-(3,4-dimethoxyphenyl)-2-propanol, (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl p-toluenesulfonate!, (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl methanesulfonate!, (S)-2-chloro-1-(3,4-dimethoxyphenyl)propane, (S)-2-bromo-1-(3,4-dimethoxyphenyl)propane and so on.

The (S)-1-(2,2-di-C₁₋₄ alkyl-1,3-benzodioxol-5-yl)-2-substituted propane derivative (3) includes, for example, (S)-1-(2,2-dimethyl-1,3-benzodioxol-5-yl)-2-propanol, (S)- 1-methyl-2-(2,2-dimethyl-1,3-benzodioxol-5-yl)ethyl p-toluenesulfonate!, (S)- 1-methyl-2-(2,2-dimethyl-1,3-benzodioxol-5-yl)ethyl methanesulfonate!, (S)-2-chloro-1-(2,2-dimethyl-1,3-benzodioxol-5-yl)propane, (S)-2-bromo-1-(2,2-dimethyl-1,3-benzodioxol-5-yl)propane, etc.

As examples of the (S)-1- 2,2-bis(C₂₋₅ alkoxycarbonyl)-1,3-benzodioxol-5-yl!-2-substituted propane derivative (4), there may be mentioned (S)- dimethyl 5-(2-hydroxypropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (S)- diethyl 5-(2-hydroxypropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (S)- dimethyl 5- 2-(p-toluenesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (S)- diethyl 5- 2-(p-toluenesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (S)- dimethyl 5- 2-(methanesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (S)- diethyl 5- 2-(methanesulfonyloxy) propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (S)- dimethyl 5-(2-chloropropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (S)- diethyl 5-(2-chloropropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (S)- dimethyl 5-(2-bromopropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (S)- diethyl 5-(2-bromopropyl)-1,3-benzodioxole-2,2-dicarboxylate! and the like.

Examples of the (S)-1-(2,2-dicarboxy-1,3-benzodioxol-5-yl)-2-substituted propane derivative (5) include (S)- disodium 5- 2-(hydroxypropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (S)- disodium 5- 2-(p-toluenesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboylate!, (S)- disodium 5- 2-(methanesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (S)- disodium 5-(2-chloropropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (S)- disodium 5-(2-bromopropyl)-1,3-benzodioxole-2,2-dicarboxylate! and others.

The (S)-1-phenyl-2-substituted propane derivative of the general formula (I) can be prepared by a variety of methods, for instance, by a chemical reaction, and can advantageously be prepared by utilizing an action of a microorganism or a preparation thereof.

Among the (S)-1-phenyl-2-substituted propane derivatives shown by the general formula (I), (a) the compound wherein X is a hydroxyl group, that is, (S)-1-phenyl-2-propanol derivative shown by the general formula (III) can easily be obtained by asymmetrical reduction of the phenylacetone derivative shown by the general formula (II), (i) with the use of a microorganism or a preparation thereof, or (ii) in a chemical method, and harvesting or recovering the product (S)-1-phenyl-2-propanol derivative.

In the method (i), the (S)-1-phenyl-2-substituted propane derivative of the general formula (I) can be obtained by permitting a microorganism or a preparation thereof to act on the phenylacetone derivative of the general formula (II) and harvesting or recovering the objective product.

The phenylacetone derivative of the general formula (II) used as a raw material can easily be obtained by a conventional manner, for example, dry distillation of a mixture of an acetic acid salt such as an acetic acid salt with an alkaline earth metal (e.g. calcium acetate and barium acetate) and a phenylacetic acid salt corresponding to the compound of the general formula (II) such as a phenyl acetic acid salt with an alkaline earth metal salt (for instance, calcium phenylacetate, barium phenylacetate, etc.) or others.

The microorganisms to be employed in accordance with the method may be any strain of microorganism that is capable of asymmetrically reducing a phenylacetone derivative shown by the general formula (II) to produce the optically active (S)-1-phenyl-2-substituted propane derivative shown by the general formula (III).

Examples of such microorganisms a strain of microorganism belonging to the genus Sphingobacterium, the genus Aeromonas, the genus Agrobacterium, the genus Aureobacterium, the genus Bacillus, the genus Cellulomonas, the genus Chromobacterium, the genus Corynebacterium, the genus Gluconobacter, the genus Jensenia, the genus Comamonas, the genus Pseudomonas, the genus Alternaria, the genus Amanita, the genus Aspergillus, the genus Cochliobolus, the genus Corynespora, the genus Dactylium, the genus Drechslera, the genus Echinopodospora, the genus Gelasinospora, the genus Gonatobotryurn, the genus Helminthosporium, the genus Mortierella, the genus Paecilomyces, the genus Phialophora, the genus Phytophthora, the genus Podospora, the genus Rhizomucor, the genus Septoria, the genus Sporormielia, the genus Stemphylium, the genus Talaromyces, the genus Torula, the genus Ustilago, the genus Westerdykella, the genus Ambrosiozyyma, the genus Dekkera, the genus Candida, the genus Clavispora, the genus Cryptococcus, the genus Debaryomyces, the genus Galactomyces, the genus Filobasidium, the genus Geotrichum, the genus Hansenula, the genus Issatchenkia, the genus Kloeckera, the genus Kluyveromyces, the genus Leucosporidium, the genus Lodderomyces, the genus Metschnikowia, the genus Myxozyma, the genus Oosporidium, the genus Pachysolen, the genus Pichia, the genus Malassezia, the genus Rhodosporidium, the genus Kondoa, the genus Rhodotorula, the genus Saccharomyces, the genus Octosporomyces, the genus Sporidiobolus, the genus Sporobolomyces, the genus Sporopachydermia, the genus Sterigmatomyces, the genus Torulaspora, the genus Torulopsis, the genus Trigonopsis, the genus Wickerhamia, the genus Wingea, the genus Zygoascus, the genus Zygosaccharomyces, the genus Zygozyma and others.

(1) The strain of microorganism belonging to the genus Sphingobacterium includes Sphingobacterium sp. IFO 13310, etc.

(2) The strain of microorganism belonging to the genus Aeromonas includes Aeromonas hydrophila subsp. proteolytiga IFO 13287, etc.

(3) The strain of microorganism belonging to the genus Agrobacterium includes Agrobacterium radiobacter IFO 12664, etc.

(4) The strain of microorganism belonging to the genus Aureobacterium includes Aureobacterium testaceum IFO 12675, etc.

(5) The strain of microorganism belonging to the genus Bacillus includes Bacillus cereus AHU 1355, etc.

(6) The strain of microorganism belonging to the genus Cellulomonas includes Cellulomonas flavigena IFO 3754, etc.

(7) The strain of microorganism belonging to the genus Chromobacterium includes Chromobacterium iodinum IFO 3558, etc.

(8) The strain of microorganism belonging to the genus Corynebacterium includes Corynebacterium aquaticum IFO 12154, etc.

(9) The strain of microorganism belonging to the genus Gluconobacter includes Gluconobacter oxydans IFO 3255, etc.

(10) The strain of microorganism belonging to the genus Jensenia includes Jensenia canicruria IFO 13914, etc.

(11) The strain of microorganism belonging to the genus Comamonas includes Comamonas acidovorans IFO 13582, etc.

(12) The strain of microorganism belonging to the genus Pseudomonas includes Pseudomonas fluorescens IFO 3081, Pseudomonas putida IFO 3738, etc.

(13) The strain of microorganism belonging to the genus Alternaria includes Alternaria japonica IFO 5244, etc.

(14) The strain of microorganism belonging to the genus Amanita includes Amanita citrina IFO 8261, etc.

(15) The strain of microorganism belonging to the genus Aspergillus includes Aspergillus awamori nakazawa IFO 4033, Aspergillus ficuum IFO 4018, Aspergillus niger AHU 7105, Aspergillus niger IFO 5374, etc.

(16) The strain of microorganism belonging to the genus Cochliobolus includes Cochliobolus miyabeanus IFO 6631, etc.

(17) The strain of microorganism belonging to the genus Corynespora includes Corynespora cassiicola IFO 6724, etc.

(18) The strain of microorganism belonging to the genus Dactylium includes Dactylium dendroides ATCC 46032, etc.

(19) The strain of microorganism belonging to the genus Drechslera includes Drechslera avenae IFO 6636, etc.

(20) The strain of microorganism belonging to the genus Echinopodospora includes Echinopodospora jamaicensis IFO 9819, etc.

(21) The strain of microorganism belonging to the genus Gelasinospora includes Gelasinospora cerealis IFO 6759, etc.

(22) The strain of microorganism belonging to the genus Gonatobotryum includes Gonatobotryum apiculatum IFO 9098, etc.

(23) The strain of microorganism belonging to the genus Helminthosporium includes Helminthosporium sigmoideum var. irregulare IFO 5273, etc.

(24) The strain of microorganism belonging to the genus Mortierella includes Mortierella isabeilina IFO 6336, etc.

(25) The strain of microorganism belonging to the genus Paecilomyces includes Paecilomyces variotii IFO 4855, etc.

(26) The strain of microorganism belonging to the genus Phialophora includes Phialophora pedrosoi IFO 6071, etc.

(27) The strain of microorganism belonging to the genus Phytophthora includes Phytophthora capsici IFO 8386, etc.

(28) The strain of microorganism belonging to the genus Podospora includes Podospora carbonaria IFO 30294, etc.

(29) The strain of microorganism belonging to the genus Rhizomucor includes Rhizomucor pusillus IFO 4578, etc.

(30) The strain of microorganism belonging to the genus Septoria includes Septoria glycines IFO 5294, etc.

(31) The strain of microorganism belonging to the genus Sporormielia includes Sporormielia isomera IFO 8538, etc.

(32) The strain of microorganism belonging to the genus Stemphylium includes Stemphylium sarciniforme IFO 7243, etc.

(33) The strain of microorganism belonging to the genus Talaromyces includes Talaromyces flavus var. flavus IFO 7231, etc.

(34) The strain of microorganism belonging to the genus Torula includes Torula jeanselmei IFO 6857, etc.

(35) The strain of microorganism belonging to the genus Ustilago includes Ustilago cynodontis IFO 7530, etc.

(36) The strain of microorganism belonging to the genus Westerdykella includes Westerdykella multispora IFO 5813, etc.

(37) The strain of microorganism belonging to the genus Ambrosiozyma includes Ambrosiozyma cicatricosa IFO 1846, Ambrosiozyma monospora IFO 1965, etc.

(38) The strain of microorganism belonging to the genus Dekkera includes Dekkera custersianus IFO 1585, etc.

(39) The strain of microorganism belonging to the genus Candida includes Candida aaseri IFO 10104, Candida atomspherica IFO 1969, Candida beechii IFO 10229, Candida diversa IFO 1091, Candida ergatensis IFO 10233, Candida fluviatilis IFO 10234, Candida fusiformate IFO 10225, Candida glabrata IFO 0622, Candida gropengiesseri IFO 0659, Candida halonitratophila IFO 1595, Candida inconspicua IFO 0621, Candida kefyr DSM 70073, Candida krusei DSM 70075, Candida lambica DSM 70090, Candida mogii IFO 0436, Candida maltosa IFO 1978, Candida melibiosica IFO 10238, Candida membranaefaciens IFO 1246, Candida oleophila JCM 2444, Candida parapsilosis IFO 1022, Candida pintolopesii var. pintolopesii IFO 0729, Candida pseudointermedia IFO 1693, Candida catenulata DSM 70136, Candida rugosa IFO 0591, Candida saitoana IFO 0768, Candida sake IFO 1149, Candida natalensis IFO 1981, Candida salmanticensis IFO 10242, Candida santamariae IFO 1982, Candida schatavii IFO 10258, Candida shehatae IFO 1983, Candida silvanorum IFO 10419, Candida sorbophila IFO 1583, Candida tenuis IFO 10315, Candida utilis IFO 0396, Candida utilis IFO 0988, Candida albicans IFO 0759, etc.

(40) The strain of microorganism belonging to the genus Clavispora includes Clavispora lusitaniae IFO 1019, etc.

(41) The strain of microorganism belonging to the genus Cryptococcus includes Cryptococcus humicolus IFO 0760, Cryptococcus neoformans IAM 4788, etc.

(42) The strain of microorganism belonging to the genus Debaryomyces includes Debaryomyces varijiae DSM 70252, etc.

(43) The strain of microorganism belonging to the genus Galactomyces includes Galactomyces reessii IFO 1112, etc.

(44) The strain of microorganism belonging to the genus Filobasidium includes Filobasidium capsuligenum IFO 1119, etc.

(45) The strain of microorganism belonging to the genus Geotrichum includes Geotrichum candidum IFO 4598, Geotrichum fermentans JCM 2467, Geotrichum fragrans JCM 2450, etc.

(46) The strain of microorganism belonging to the genus Hansenula includes Hansenula polymorpha ATCC 26012, Hansenula capsulata DSM 70269, Hansenula glucozyma DSM 70271, Hansenula wickerhamii DSM 70280, etc.

(47) The strain of microorganism belonging to the genus Issatchenkia includes Issatchenkia scutulata var. scutulata IFO 10070, etc.

(48) The strain of microorganism belonging to the genus Kloeckera includes Kloeckera africana IFO 0869, etc.

(49) The strain of microorganism belonging to the genus Kluyveromyces includes Kluyveromyces lactis IFO 0433, Kluyveromyces marxianus DSM 70800, Kluyveromryces polysporus DSM 70294, etc.

(50) The strain of microorganism belonging to the genus Leucosporidium includes Leucosporidium scottii IFO 1924, etc.

(51) The strain of microorganism belonging to the genus Lodderomyces includes Lodderomyces elongisporus IFO 1676, etc.

(52) The strain of microorganism belonging to the genus Metschnikowia includes Metschnikowia bicuspidata IFO 1408, Metschnikowia pulcherrima DSM 70336, Metschnikowia reukaufii DSM 70880, etc.

(53) The strain of microorganism belonging to the genus Myxozyma includes Myxozyma lipomycoides IFO 10350, etc.

(54) The strain of microorganism belonging to the genus Oosporidium includes Oosporidium margaritiferum IFO 1208, etc.

(55) The strain of microorganism belonging to the genus Pachysolen includes Pachysolen tannophilus IFO 1007, etc.

(56) The strain of microorganism belonging to the genus Pichia includes Pichia cellobiosa DSM 2147, Pichia farinosa IFO 1163, Pichia lindnerii DSM 70718, Pichia ohmeri DSM 70815, Pichia thermotolerans IFO 10025, Pichia pastoris DSM 70382, Pichia trehalophila DSM 70391, Pichia carsonii DSM 70392, Pichia subpelliculosa IFO 0808, etc.

(57) The strain of microorganism belonging to the genus Malassezia includes Malassezia furfur IFO 0656, etc.

(58) The strain of microorganism belonging to the genus Rhodosporidium includes Rhodosporidium diobovatum IFO 1830, Rhodosporidium toruloides IFO 1638, etc.

(59) The strain of microorganism belonging to the genus Kondoa includes Kondoa malvinella IFO 1936, etc.

(60) The strain of microorganism belonging to the genus Rhodotorula includes Rhodotorula glutinis AHU 3454, Rhodotorula rubra IFO 0383, etc.

(61) The strain of microorganism belonging to the genus Saccharomyces includes Saccharomyces rouxii IAM 0487, etc.

(62) The strain of microorganism belonging to the genus Octosporomyces includes Octosporomyces octosporus IFO 0353, etc.

(63) The strain of microorganism belonging to the genus Sporidiobolus includes Sporidiobolus johnsonii IFO 6903, Sporidiobolus pararoseus IFO 1104, Sporidiobolus salmonicolor IFO 1845, etc.

(64) The strain of microorganism belonging to the genus Sporobolomyces includes Sporobolomyces pararoseus IFO 1036, etc.

(65) The strain of microorganism belonging to the genus Sporopachydermia includes Sporopachydermia lactactivora IFO 1867, etc.

(66) The strain of microorganism belonging to the genus Sterigmatomyces includes Sterigmatomyces elviae DSM 70852, etc.

(67) The strain, of microorganism belonging to the genus Torulaspora includes Torulaspora delbrueckii IFO 0381, etc.

(68) The strain of microorganism belonging to the genus Torulopsis includes Torulopsis nemodendra DSM 70647, etc.

(69) The strain of microorganism belonging to the genus Trigonopsis includes Trigonopsis variabilis IFO 0755, etc.

(70) The strain of microorganism belonging to the genus Wickerhamia includes Wickerhamia fluorescens DSM 70715, Wickerhamiella domercquii IFO 1857, etc.

(71) The strain of microorganism belonging to the genus Wingea includes Wingea robertsii IFO 1277, etc.

(72) The strain of microorganism belonging to the genus Zygoascus includes Zygoascus hellenicus IFO 1575, etc.

(73) The strain of microorganism belonging to the genus Zygosaccharomyces includes Zygosaccharomyces bailii IFO 0468, Zygosaccharomyces bisporus DSM 70415, etc.

(74) The strain of microorganism belonging to the genus Zygozyma includes Zygozyma oligophaga IFO 10360, etc.

For the purposes of the invention, any of wild strains, mutants and recombinant strains which can be obtained by a genetic engineering technique such as cell fusion or gene manipulation can suitably be used, as far as having the above mentioned ability or capability.

The microorganisms identified hereinabove by IFO numbers are described in the "List of Cultures Ed. 9" published by Institute for Fermentation, Osaka (IFO), Japan and are available from the same Institute. The microorganisms designated by JCM numbers are listed in "Catalogs of Microbial Strains Ed. 5 (1992)" published by the Culture Collection of The Institute of Physical and Chemical Research, Japan and available from the same Culture Collection. The microorganism designated by DSM numbers are listed in "Catalogue of strains (1989)" published by the Deutsch Sammlung von Mikroorganismen (DSM) and are available from the same organization. The yeast identified by ATCC number (Hansenula polymorpha ATCC 26012) is listed in "Catalogue of Yeasts, Ed. 18 (1990)" and the filamentous fungus designated by ATCC number (Dactylium dedroides ATCC 46032) is listed in "Catalogue of Filamentous fungi, Ed. 18 (1991)" each published by the American Type Culture Collection (ATCC) and are respectively available from the same organization. The microorganisms titled by IAM numbers are available from Institute of Applied Microbiology, Tokyo University, Japan. The microorganisms identified by AHU numbers are available from Faculty of Agriculture, Hokkaido University, Japan.

The medium which is used for growing the strain for use in the invention is not critical in composition only if the selected strain may grow and multiply therein. The medium may frequently be a fluid medium containing sources of carbon and nitrogen and other nutrients. Any carbon source which the strain can utilize may be employed. As the sources of carbon, there may be employed various carbohydrates or saccharides such as glucose, fructose, sucrose, dextrin, starch, etc.; alcohols such as sorbitol, methanol, ethanol, glycerol, etc.; organic acids such as fumaric acid, citric acid, acetic acid, propionic acid, etc. and the corresponding salts; hydrocarbons such as paraffin; and various mixtures thereof. The sources of nitrogen include, for instance, inorganic acid ammonium salts such as ammonium chloride, ammonium sulfate, ammonium phosphate, etc.; organic acid ammonium salts such as ammonium fumarate, ammonium citrate, etc.; inorganic or organic nitrogen-containing materials such as meat extract, yeast extract, malt extract, peptone (polypeptone), corn steep liquor, casein hydrolysate, urea, etc.; and various mixtures thereof.

In the medium, there may be incorporated appropriate amounts of those nutrients which are commonly employed in the cultivation of microorganisms, such as inorganic salts, trace metal salts and vitamins. Where necessary, there may also be incorporated factors which may promote growth of the strain used and/or factors which may augment its ability to produce the object compound of the invention, as well as a buffer substance which may assist in the maintenance of the medium at a given pH.

The cultivation of the microorganism is carried out under conditions optimal for the growth of the particular strain, for example at a medium pH in the range of about 2.0 to 9.5, preferably about 3 to 8, and an incubation temperature in the range of about 20 to 45° C., preferably about 25 to 37° C. The cultivation may be aerobic or anaerobic. The cultivation time is, for example, about 5 to 120 hours, preferably about 12 to 72 hours.

The method of asymmetric reduction is not critical so far as the function of a microorganism or a preparation thereof is acted on the phenylacetone derivative of the general formula (II) to produce the (S)-1-phenyl-2-substituted propane derivative of the general formula (I), and may, for example, be whichever of the following alternatives: (1) a technique adding the phenylacetone derivative to the culture medium where the microorganism is cultivated, (2) a technique adding or mixing the phenylacetone derivative with a culture broth as such to conduct the reaction, (3) a technique which comprises separating the microbial cells from the culture broth, e.g. by centrifugation, resuspending the cells, either as they are or after washing, in a buffer solution, water or the like, and adding the phenylacetone derivative to the resulting cell suspension to treat the mixture therewith.

There are cases in which this reaction proceeds with advantage of a higher yield of the objective optically active compound in the presence of a carbon source such as glucose, sucrose, ethanol, methanol or paraffin which serves as an energy source.

In the reaction, wet viable cells as such can be used, or a treated preparation of cells such as disrupted cells, acetone-treated cells, lyophilized cells can also be employed. These cells or preparation thereof can be employed as immobilized by known techniques such as the polyacrylamide gel method, sulfur-containing polysaccharide gel method (e.g. carrageenin gel method), alginic acid gel method, agar gel method and so on. The enzyme purified from such a cell preparation can also be used. The enzyme can be obtained with the use of known purification processes in a suitable combination.

The corresponding phenylacetone derivative can be used as it is or in the form of a solution, suspension or dispersion containing a suitable solvent. As the solvent, water or an organic solvent which will not interfere with the reaction can be employed. A suspension or a dispersion prepared with a surfactant can also be used when necessary. The phenylacetone derivative may be added in bolus at the beginning of the reaction or in several installments.

The optimal cell concentration of the reaction system can be selected from the range where the yield and the optical purity of the desired optically active compound will not be adversely affected. A typical cell concentration may for example be, on a dry cell basis, about 0.1 to 500 g/liter and preferably about 1 to 300 g/liter. The concentration of the substance phenylacetone derivative is not particularly restricted and is, for example, about 0.01 to 20% by weight and preferably about 0.1 to 10% by weight.

The reaction conditions of the asymmetric reduction can be selected from the ranges that will not detract from the yield of the object compound. For example, the pH of the reaction system can be selected from the range of pH about 2 to 10 and preferably pH about 3 to 8. The reaction temperature is selected from the range of, for example, about 10 to 60° C. and preferably from about 20 to 40° C. and more preferably from about 20 to 35° C. The reaction can be conducted with stirring or under stationary conditions for about 1 to 120 hours.

Thus, when permitting the microorganism or a preparation thereof to act on the phenylacetone derivative, the asymmetric reduction can proceed smoothly or advantageously to produce the corresponding 1-phenyl-2-propanol derivative having an (S)-configuration with a high selectivity.

The (S)-1-phenyl-2-propanol derivative of the general formula (III) produced by the reaction can be recovered or harvested by the separation and purification procedures generally known. For example, the (S)-1-phenyl-2-propanol derivative having a high optical purity can be easily obtained by subjecting the reaction mixture, directly or after separation of the cells, to the conventional purification procedure such as membrane separation, extraction with an organic solvent, crystallization, recrystallization, column chromatography, vacuum concentration and distillation. The optical purity of optically active compound can be measured by high performance liquid chromatography (HPLC) using an optical resolution column.

In the (S)-1-phenyl-2-substituted propane derivatives shown by the general formula (I), (b) the compound wherein X is an optionally substituted alkylsulfonyloxy group, an optionally substituted arylsulfonyloxy group or a halogen atom, that is a compound shown by the general formula (IV), can easily or readily be obtained from the compound of the formula (III) by selecting an reagent, for example a sulfonylating agent or a halogenating agent, a catalyst and reaction conditions from the range where the reaction proceeds with retention in stereochemistry. Such reaction is illustrated, for instance, by the following scheme: ##STR9##

The sulfonylating agent includes a variety of conventional sulfonylating agents which can convert a hydroxyl group into an alkylsulfonyloxy or arylsulfonyloxy group, for example, an optionally substituted alkylsulfonyl halide or an optionally substituted arylsulfonyl halide.

As the optionally substituted alkylsulfonyl halide and the optionally substituted arylsulfonyl halide, those corresponding to X may be employed. Such optionally substituted alkylsulfonyl halide include, for instance, an alkylsulfonyl halide having 1 to 4 carbon atoms which may be substituted with a substituent such as a halogen atom on the alkyl group, including methanesulfonyl chloride, methanesulfonyl bromide, ethanesulfonyl chloride, ethanesulfonyl bromide, trichloromethanesulfonyl chloride, trifluoromethanesulfonyl chloride, and the like. Examples of the optionally substituted arylsulfonyl halide include an arylsulfonyl halide having 6 to 20 carbon atoms, preferably 6 to 15 carbon atoms, which may have a substituent such as an alkyl group, a nitro group and a halogen atom on the aromatic ring, for example, benzenesulfonyl chloride, benzenesulfonyl bromide, o-toluenesulfonyl chloride, p-toluenesulfonyl chloride, p-toluenesulfonyl bromide, m-nitrobenzenesulfonyl chloride, p-nitrobenzenesulfonyl chloride, p-chlorobenzenesulfonyl chloride, p-bromobenzenesulfonyl chloride, naphthalenesulfonyl chloride and so on.

The reaction of the (S)-1-phenyl-2-propanol derivative of the general formula (III) with the sulfonylating agent can be carried out, usually in the presence of a base at a temperature of, for instance, about -20° C. to 100° C., preferably about -10° C. to 40° C., and more preferably about 0° C. to 30° C. When the reaction temperature is lower than -20° C., the reaction rate is decreased, and when the reaction temperature exceeds 100° C., occurrence of a side reaction tends to be enhanced.

The base includes inorganic bases and organic bases. As examples of the inorganic bases, there may be mentioned alkali metal hydroxides such as sodium hydroxide, potassium hydroxide and lithium hydroxide; alkaline earth metal hydroxides such as magnesium hydroxide, calcium hydroxide and barium hydroxide; alkali metal carbonates such as sodium carbonate, potassium carbonate and lithium carbonate; alkaline earth metal carbonate such as magnesium carbonate, calcium carbonate and barium carbonate; alkali metal hydrogencarbonates such as sodium hydrogencarbonate and potassium hydrogencarbonate. The organic bases include, for example, metal alkoxides such as alkali metal alkoxides (for example, a sodium or potassium C₁₋₄ alkoxide such as sodium methoxide, sodium ethoxide, sodium propoxide, sodium butoxide, potassium methoxide, potassium ethoxide, potasium propoxide and potasium butoxide, etc.); primary amines such as an alkylamine (e.g. a C₁₋₈ alkylamine such as methylamine, ethylamine, propylamine, butylamine, etc.); secondary amines such as chain amines including an dialkylamine (e.g. a di-C₁₋₈ alkylamine such as dimethylamine, diethylamine, dipropylamine, diisopropylamine, dibuthylamine, diisobutylamine, di-s-butylamine, di-t-butylamine, dipentylamine, dihexylamine, diheptylamine, dioctylamine, etc.), and cyclic amines such as pipecoline, piperidine, morpholine, pyrrolidine, etc.; tertiary amines such as a trialkylamine (e.g. a tri-C₁₋₈ alkylamine such as trimethylamine, triethylamine, tripropylamine, tributylamine, etc.), alkanolamines such as N,N-di-C₁₋₄ alkyl alkanolamine (e.g. N,N-dimethylethanolamine, and the like), N,N-dimethylaniline, 4-dimethylaminopyridine, N-methylmorpholine, N-methylpiperidine, and others; nitrogen-containing heterocycric compounds such as pyridine, quinoline, picoline, and others. As the base, the organic bases such as pyridine may frequently be employed.

The reaction may be conducted in an inert solvent. As the solvent, there may be mentioned, for instance, aromatic hydrocarbons such as benzene, toluene, xylene and ethylbenzene; aliphatic hydrocarbons such as pentane, hexane, heptane and octane; alicyclic hydrocarbons such as cyclohexane and methylcyclohexane; halogenated hydrocarbons such as carbon tetrachloride, chloroform, dichloromethane and 1,2-dichloroethane; ethers such as diethyl ether, dibutyl ether, dioxane and tetrahydrofuran; ketones such as acetone and methyl ethyl ketone; esters such as methyl acetate and ethyl acetate; aprotic polar solvents such as acetonitrile, N,N-dimethylformamide and dimethyl sulfoxide.

The using amount of the sulfonylating agent can be selected from a suitable range depending on the reaction rate and economic factors, and is usually about 0.9 gram equivalent or more, preferably about 0.9 to 1.5 gram equivalents and more preferably about 1.1 to 1.3 gram equivalents, relative to 1 gram equivalent of the (S)-1-phenyl-2-propanol derivative of the general formula (III).

By the reaction of the (S)-phenyl-2-propanol derivative with the sulfonylating agent, the corresponding (S)-2-alkylsulfonyloxy-1-phenylpropane derivative or (S)-2-arylsulfonyloxy-1-phenylpropane derivative can selectively be produced with a good yield.

As the halogenating agent, there may be mentioned, for instance, conventional halogenating agents usable when halogenating an optically active alcohol wherein a hydroxyl group is bonded to an asymmetric carbon with retention of the configuration. Examples of such halogenating agents include thionyl chloride, thionyl bromide and the like.

The reaction of the (S)-1-phenyl-2-propanol derivative with the halogenating agent can be carried out at a temperature of, for example, about -20° C. to 150° C. and preferably about 10° C. to 120° C. The reaction conducted at a temperature lower than -20° C. decreases the reaction rate, and the reaction carried out at a temperature exceeding 150° C. tends to cause a side reaction. The reaction may be conducted in an inert solvent. The solvent exemplified as above can also be used in this reaction. The preferred solvent includes a solvent, which advantageously proceed the reaction with retention of the configuration, for example, a solvent containing an oxygen atom or a sulfur atom such as ethers including, for instance, dioxane, diethyl ether, dipropyl ether, diisopropyl ether, 1,2-dimethoxyethane, anisole, tetrahydrofuran, and the like. The halogenating agent can also be used as the solvent.

The amount of the halogenating agent relative to 1 gram equivalent of the (S)-1-phenyl-2-propanol derivative of the general formula (III) is, for instance, about 0.9 gram equivalent or more and preferably about 0.9 to 1.5 gram equivalents. In order to proceed the reaction smoothly, a reaction accelerator such as sodium chloride, sodium bromide and N,N-dimethylformamide; the above mentioned base or the like can be added to the reaction system.

By the reaction of the (S)-1-phenyl-2-propanol derivative of the general formula (III) and the halogenating agent, the corresponding (S)-2-halo-1-phenylpropane derivative can selectively and efficiently be produced.

The (S)-1-phenyl-2-substituted propane derivative of the general formula (IV) produced by the sulfonylation or halogenation as mentioned above can be recovered by conventional separation and purification procedures. For example, the (S)-1-phenyl-2-substituted propane derivative having a high optical purity can be easily obtained by subjecting the reaction mixture to the conventional purification procedure such as pH adjustment or control of the reaction mixture, extraction with an organic solvent, crystallization, recrystallization, vacuum concentration, column chromatography and distillation.

The (S)-1-phenyl-2-substituted propane derivative of the general formula (IV) thus obtained can advantageously be employed as an intermediate for synthesis of the (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative usable as a medicinal compound or an intermediate thereof.

In the (S)-1-phenyl-2-substituted propane derivatives of the general formula (I), (c) other compounds than the compounds of the general formula (III) or (IV), that is, the compounds wherein X is a hydroxyl group which is protected by a protective group can readily or easily be obtained by protecting the hydroxyl group of the compound of the general formula (II) with the protective group in accordance with a conventional manner using a protective reagent. The compound thus obtained can appropriately be used when the protection of the hydroxyl group is required in chemical reaction for producing another derivative from the compound of the general formula (I).

In the (S)-1-phenyl-2-substituted propane derivatives of the general formula (I) of the present invention, R¹, R² or both can be converted from one substituent to another by a conventional technique.

For example, the (S)-1-phenyl-2-substituted propane derivative of the general formula (I) where R¹ and R² are both methyl groups can easily be converted to the compound where R¹ and R² incorporatively form the group shown by the formula (IX) in accordance with the following scheme. ##STR10## wherein R¹¹, R¹² and R¹³ respectively represent an optionally substituted alkyl group; X^(a) and X^(b) are independently a halogen atom; and R³, R⁴, R⁵ and X have the same meanings as defined above.

In the reaction, a compound of the formula (Ic) having the group of the formula (IX) where R^(a) and R^(b) are both optionally substituted alkoxycarbonyl groups, can be prepared by allowing a demethylating agent such as BBr₃ to react with the compound of the general formula (I) where R¹ and R² are both methyl groups, that is, the compound of the formula (Ia), and allowing a dihalomalonic acid ester shown by the formula (XI) such as diethyl dibromomalonate to react with the demethylated compound of the formula (Ib) in the presence of a base such as potassium carbonate. The resultant compound (Ic) can be introduced to a compound of the formula (Id) having the group of the formula (IX) where R^(a) and R^(b) are both hydroxyl groups by using a reducing agent such as lithium borohydride. When allowing a halogenated alkyl of the formula (XII) to react with the compound of the formula (Id) in the presence of a base such as sodium hydride, a compound of the formula (Ie) having the group of the formula (XI) where R^(a) and R^(b) are respectively an optionally substituted alkoxymethyl group can be obtained.

Further, hydrolysis of the compound of the formula (Ic) in accordance with a conventional hydrolyzing method such as alkali hydrolysis using an alkali including an alkali metal hydroxide (e.g. sodium hydroxide) or the like can easily or readily afford a compound of the formula (If) having the group of the formula (IX) wherein R^(a) and R^(b) are, the same or different, a carboxyl group or a salt thereof.

With regard to the method, the disclosures and descriptions in the above mentioned U.S. Pat. No. 5,061,727 and J. Med. Chem., 35, 3081 (1992) can be referred, and these disclosures and descriptions can be incorporated with the disclosure of the present specification.

The process for producing the (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative shown by the general formula (VI) of the present invention is characterized by allowing the (R)-2-amino-1-phenylethanol derivative of the general formula (V) to react with the (S)-1-phenyl-2-substituted propane derivative of the general formula (IV) with inversion in stereochemistry to produce the objective compound of the formula (VI).

The lower alkyl group, lower haloalkyl group, lower alkoxy group or halogen atom in R⁶, R⁷, R⁸, R⁹ and R¹⁰ of the general formula (V) may be referred to the lower alkyl group or the like exemplified above. As the substituent R⁹, a lower haloalkyl group such as a C₁₋₄ haloalkyl group, a halogen atom, a nitro group or the like, particularly a halogen atom such as chlorine atom is preferable. Preferred examples of R⁶, R⁷, R⁸ and R¹⁰ include a hydrogen atom and a C₁₋₄ alkyl group, specifically a hydrogen atom.

The protective group for hydroxyl group in Z of the general formula (V) may refer to, for example, a group mentioned as the protective group for hydroxyl group in the explanation for R¹, R² and X.

Typical examples of Z include a hydrogen atom, (A) a group which forms an ether bond with an oxygen atom, particularly, C₁₋₄ alkyl group, an optionally substituted 5- to 6-membered heterocyclic group having an oxygen atom or a sulfur atom as a hetero atom, and an optionally substituted silyl group, (B) a group which forms an ester bond with an oxygen atom such as an optionally substituted C₁₋₆ acyl group, an optionally substituted C₇₋₁₆ acyl group having an aromatic ring and an optionally substituted acyl group having a heterocyclic ring, and (C) a group which forms a carbonate with an oxygen atom such as an optionally substituted C₂₋₅ alkoxycarbonyl group, an optionally substituted C₈₋₂₀ aralkyloxycarbonyl group and an optionally substituted C₇₋₂₀ aryloxycarbonyl group. Particularly, a hydrogen atom can advantageously be used as Z.

In the present invention, the protective group for hydroxyl group, introduction of the protective group to hydroxyl group and cleavage of the protective group may, for example, be referred to and incorporated with "Protective Groups in Organic Synthesis" (T. W. Greene, A Wiley-Interscience Publication, John Wiley & Sons (1981)).

As practical examples of the (R)-2-amino-1-phenylethanol derivative shown by the general formula (V), there may be mentioned (a) (R)-2-amino-1-phenylethanol; (b) an (R)-2-amino-1-(3-nitrophenyl)ethanol derivative such as (R)-2-amino-1-(3-nitrophenyl)ethanol, (R)-2-amino-1-(2-methyl-3-nitrophenyl)ethanol, etc.; (c) an (R)-2-amino-1-(3-halophenyl)ethanol derivative such as (R)-2-amino-1-(3-chlorophenyl)ethanol, (R)-2-amino-1-(2,3-dichlorophenyl)ethanol, (R)-2-amino-1-(3,4-dichlorophenyl)ethanol, (R)-2-amino-1-(3-bromophenyl)ethanol, (R)-2-amino-1-(2,3-dibromophenyl)ethanol, (R)-2-amino-1-(3,4-dibromophenyl)ethanol, (R)-2-amino-1-(3-fluorophenyl)ethanol, (R)-2-amino-1-(2,3-difluorophenyl)ethanol, (R)-2-amino-1-(3,4-difluorophenyl)ethanol and the like; (d) an (R)-2-amino-1-(3-C₁₋₄ haloalkyl-phenyl)ethanol derivative such as (R)-2-amino-1-(3-chloromethylphenyl)ethanol, (R)-2-amino-1- 3-(2-chloroethyl)phenyl!ethanol, (R)-2-amino-1- 3-(4-chlorobutyl)phenyl!ethanol, (R)-2-amino-1-(3-trichloromethylphenyl)ethanol, (R)-2-amino-1-(3-trifluoromethylphenyl)ethanol, (R)-2-amino-1- 3-(1,1,2,2,2-pentafluoroethyl)phenyl!ethanol, etc.; (e) an (R)-2-amino-1-(3-C₁₋₄ alkoxy-phenyl)ethanol derivative such as (R)-2-amino-1-(3-methoxyphenyl)ethanol, (R)-2-amino-1-(3-methoxy-4-chlorophenyl)ethanol, (R)-2-amino-1-(3-methoxy-4-methylphenyl)ethanol, (R)-2-amino-1-(3-ethoxyphenyl)ethanol; (f) an (R)-2-amino-1-(3-C₁₋₄ alkyl-phenyl)ethanol derivative such as (R)-2-amino-1-(3-methylphenyl)ethanol, (R)-2-amino-1-(3-ethylphenyl)ethanol, (R)-2-amino-1-(3-propylphenyl)ethanol, (R)-2-amino-1-(3-t-butylphenyl)ethanol, etc.; (g) an (R)-2-amino-1-(2-substituted phenyl)ethanol derivative such as (R)-2-amino-1-(2-chlorophenyl)ethanol, (R)-2-amino-1-(2-bromophenyl)ethanol, (R)-2-amino-1-(2-fluorophenyl)ethanol, (R)-2-amino-1-(2-trifluoromethylphenyl)ethanol, (R)-2-amino-1-(2-methoxyphenyl)ethanol, (R)-2-amino-1-(2-ethoxyphenyl)ethanol, (R)-2-amino-1-(2-methylphenyl)ethanol, (R)-2-amino-1-(2-ethylphenyl)ethanol), (R)-2-amino-1-(2-propylphenyl)ethanol, (R)-2-amino-1-(2-t-butylphenyl)ethanol and the like; (h) an (R)-2-amino-1-(4-substituted phenyl)ethanol derivative such as (R)-2-amino-1-(4-chlorophenyl)ethanol, (R)-2-amino-1-(4-bromophenyl)ethanol, (R)-2-amino-1-(4-fluorophenyl)ethanol, (R)-2-amino-1-(4-trifluoromethylphenyl)ethanol, (R)-2-amino-1-(4-methoxyphenyl)ethanol, (R)-2-amino-1-(4-ethoxyphenyl)ethanol, (R)-2-amino-1-(4-methylphenyl)ethanol, (R)-2-amino-1-(4-ethylphenylethanol), (R)-2-amino-1-(4-propylphenyl)ethanol, (R)-2-amino-1-(4-t-butylphenyl)ethanol, and so on.

The (R)-2-amino-1-phenylethanol derivative of the general formula (V) can be obtained by, for instance, subjecting the corresponding racemic 2-amino-1-phenylethanol derivative to a conventional optical resolution. For example, the compound can readily be obtained by allowing an optically active carboxylic acid such as an amino acid (e.g. D-alanine) derivative where the amino group is protected (e.g. N-(t-butoxycarbonyl)-D-alanine, etc.) to react with the racemic derivative to form a diastereomeric salt and recrystallizing the objective compound from the salt. The racemic 2-amino-1-phenylethanol derivative can be prepared by a conventional manner, for instance, allowing a trialkylsilylcyanide such as trimethylsilylcyanide to react with the corresponding benzaldehyde derivative in the presence of a Lewis acid such as anhydrous aluminum chloride to produce an o-trialkylsilylmandelonitrile derivative such as o-trimethylsilylmandelonitrile derivative, subjecting the resultant compound to treatment with a reducing agent such as sodium borohydride and to hydrolysis with an acid, and, when necessary, protecting the hydroxyl group with a suitable protective group.

The reaction of the compound of the general formula (V) and the compound of the general formula (IV) can be carried out, by selecting a reagent, a catalyst and reaction conditions in a suitable range as far as the reaction can be proceeded with inversion of the configuration, and, for example, at about 0 to 150° C. and preferably about 20 to 120° C. If the reaction temperature is lower than 0° C., the reaction rate is decreased, and if it exceeds 150° C., a side reaction is liable to occur.

The reaction may preferably be carried out in the presence of a base. A use of the base may increase the optical purity of the object compound. As the base, the base mentioned above can be employed. Preferred examples of the base include organic bases, particularly secondary amines and tertiary amines. Among them, chain secondary amines, specifically dialkylamines such as di-C₁₋₈ alkylamines can advantageously be employed. When such dialkylamine is used, the yield of the objective compound can remarkably be increased. Further, among cyclic amines as above, use of such amines which are bulky, for example pipecoline, may occasionally afford a high yield of the compound.

The amount of the base is, for example, about 0.5 to 10 gram equivalents, preferably about 1.0 to 5 gram equivalents and more preferably about 1.2 to 3.5 gram equivalents relative to 1 mol of the compound of the general formula (IV).

The reaction may be conducted in an inert solvent as mentioned above. Preferred examples of the solvent include hydrocarbons such as aromatic hydrocarbons, aliphatic hydrocarbon and alicyclic hydrocarbons.

The amount of the compound of the general formula (IV) can be selected from a suitable range with regard to the reaction rate and economical factors, and is generally about 0.3 to 1.5 gram equivalents and preferably about 0.5 to 1.3 gram equivalents, and more preferably about 0.8 to 1.2 gram equivalents relative to 1 mole of the compound of the general formula (V).

According to this method, the amino group of the (R)-2-amino-1-phenylethanol derivative may attack the carbon atom on the 2-position of the (S)-1-phenyl-2-substituted propane derivative of the general formula (IV) from the opposite direction against the substituent Y, and, thus, a substitution reaction with inversion can smoothly proceed stereoselectively. Therefore, the corresponding (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative of the general formula (VI) or a salt thereof with a by-produced acid HY, wherein Y has the same meaning as defined above, can be produced with a high reaction yield and optical yield.

The (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative and a salt thereof thus obtained can selectively react with the β₃ -receptor in vivo to decrease or reduce blood sugar significantly and to remarkably restrain or suppress obesity. The pharmacological activity in the (R,R)-isomer is extremely higher than those in the other optical isomers. (R,R)- disodium 5- 2- 2-(3-chlorophenyl)-2-hydroxyethyl!amino!propyl!-1,3-benzodioxole-2,2-dicarboxylate! shows, for example, a higher activity than the corresponding (S,S)-enantiomer by a factor of 47 (see the above-mentioned U.S. Patent).

When the corresponding (R)-enantiomer is used instead of the (S)-1-phenyl-2-substituted propane derivative in the reaction, the object compound (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative can hardly be produced. Further, use of the racemic 1-phenyl-2-substituted propane derivative produces the objective compound only with a yield of 50% at most, and an isolating process for isolating and removing a by-produced optical isomer is required.

As described above, the (S)-1-phenyl-2-substituted propane derivative of the present invention is remarkably usable and effective intermediate to selectively obtain the (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative efficiently with a high yield, thus the (S)-enantiomer is remarkably more usable than the corresponding (R)-enantiomer and the racemic form.

Further, the (S)-1-phenyl-2-substituted propane derivative of the formula (I) of the invention, differing from the (R)-1-methyl-2-phenylethylamine derivative, does not have an antihypnotic or arousal action, therefore is easy to handle or treat and suited for a use in commercial production.

R¹, R² or the both of the compound of the general formula (VI) can be converted from one substituent to another by a conventional manner. As such manner, the methods explained in R¹ and R² of the compound of the general formula (I) may be referred to.

For example, (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative of the general formula (VI) where R¹ and R² are both methyl groups can easily be converted to the compound where R¹ and R² incorporatively form the group shown by the formula (IX) in accordance with the above mentioned method. With regard to the method, the disclosures and descriptions in the above mentioned U.S. Pat. No. 5,061,727 and J. Med. Chem., 35, 3081 (1992) can be referred and incorporated with the present specification.

In the reaction, a compound having the group of the formula (IX) where R^(a) and R^(b) are both optionally substituted alkoxycarbonyl groups, can be prepared by allowing a demethylating agent such as BBr₃ to react with the compound of the general formula (VI) where R¹ and R² are both methyl groups for demethylation, and allowing a dihalomalonic acid ester shown by the formula (XI) such as diethyl dibromomalonate to react with the demethylated compound in the presence of a base such as potassium carbonate. The resultant compound can be introduced to a compound having the group of the formula (IX) where R^(a) and R^(b) are both hydroxyl groups by using a reducing agent such as lithium borohydride. When allowing an alkyl halide of the formula (XII) to react with the resulting compound in the presence of a base such as sodium hydride, a compound having the group of the formula (IX) where R^(a) and R^(b) are respectively an optionally substituted alkoxymethyl group can be prepared.

Further, hydrolysis of the compound having the group of the formula (IX) where R^(a) and R^(b) are respectively an optionally substituted alkoxycarbonyl group, in accordance with a conventional hydrolyzing method such as alkali hydrolysis using an alkali such as an alkali metal hydroxide (e.g. sodium hydroxide) or the like can easily or readily afford a compound having the group of the formula (IX) wherein R^(a) and R^(b) are, the same or different, a carboxyl group or a salt thereof.

The (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative of the general formula (VI) or a salt thereof produced in the above-mentioned reaction can be recovered by a conventional isolation and purification technique. For instance, the (R,R)-1-phenyl-2- (2-phenyl-1-methylethly)amino!ethanol derivative or a salt thereof having a high optical purity can easily or readily be obtained by subjecting the reaction mixture, if necessary after adjusting to alkaline, to the conventional purification procedure such as extraction with an organic solvent, vacuum concentration, column chromatography, distillation, crystallization and recrystallization.

The (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative or a salt thereof can advantageously be used, as intact or, where necessary, subjected to a suitable chemical modification, as a medicament such as an anti-obesity agent and an anti-diabetic agent. The processes for such chemical modification may be referred to the descriptions and disclosures in, for example, the above-mentioned U.S. Pat. No. 5,061,727, J. Med. Chem., 35, 3081 (1992) and "Protective groups in Organic Synthesis" (T. W. Greene, A Wiley-Interscience Publication, John Wiley & Sons (1981)).

The (R)-1-phenyl-2-substituted propane derivative shown by the general formula (VII) and production thereof are illustrated hereinbelow.

As examples and preferred R¹ to R⁵ and X of the general formula (VII), there may be mentioned the substituents as mentioned above for the general formula (I).

Among (R)-1-phenyl-2-substituted propane derivatives of the general formula (VII), preferred examples include compounds where R¹ and R² are, the same or different, (i) a hydrogen atom, a C₁₋₄ alkyl group (specifically a methyl group) or (ii) R¹ and R² incorporatively form an optionally substituted methylene group of the formula (IX) wherein R^(a) and R^(b) are respectively a carboxyl group or a salt thereof, or a C₂₋₅ alkoxycarbonyl group; R³, R⁴, and R⁵ are independently a hydrogen atom or a C₁₋₄ alkyl group; and X is a hydroxyl group, a C₁₋₂ alkylsulfonyloxy group, a C₆₋₁₅ arylsulfonyloxy group or a halogen atom.

Practical examples of the (R)-1-phenyl-2-substituted propane derivative shown by the general formula (VII) can refer the examples of the corresponding (S)-1-phenyl-2-substituted propane derivative of the general formula (I) as mentioned above. Such examples include (1) an (R)-1-(3,4-dihydroxyphenyl)-2-substituted propane derivative, (2) an (R)-1-(3,4-di-C₁₋₄ alkoxyphenyl)-2-substituted propane derivative, (3) an (R)-1-(2,2-di-C₁₋₄ alkyl-1,3-benzodioxol-5-yl)-2-substituted propane derivative, (4) an (R)-1- 2,2-bis(C₂₋₅ alkoxycarbonyl)-1,3-benzodioxol-5-yl!-2-substituted propane derivative and (5) an (R)-1-(2,2-dicarboxy-1,3-benzodioxol-5-yl)-2-substituted propane derivative.

As the (1) (R)-1-(3,4-dihydroxyphenyl)-2-substituted propane derivative, there may be mentioned, for instance, (R)-1-(3,4-dihydroxyphenyl)-2-propanol, (R)- 2-(3,4-dihydroxyphenyl)-1-methylethyl p-toluenesulfonate!, (R)- 2-(3,4-dihydroxyphenyl)-1-methylethyl methanesulfonate!, (R)-2-chloro-1-(3,4-dihydroxyphenyl)propane, (R)-2-bromo-1-(3,4-dihydroxyphenyl)propane and the like.

Examples of the (2) (R)-1-(3,4-di-C₁₋₄ alkoxyphenyl)-2-substituted propane derivative include (R)-1-(3,4-dimethoxyphenyl)-2-propanol, (R)- 2-(3,4-dimethoxyphenyl)-1-methylethyl p-toluenesulfonate!, (R)- 2-(3,4-dimethoxyphenyl)-1-methylethyl methanesulfonate!, (R)-2-chloro-1-(3,4-dimethoxyphenyl)propane, (R)-2-bromo-1-(3,4-dimethoxyphenyl)propane and so on.

The (3) (R)-1(2,2-di-C₁₋₄ alkyl-1,3-benzodioxol-5-yl)-2-substituted propane derivative includes, for example, (R)-1-(2,2-dimethyl-1,3-benzodioxol-5-yl)-2-propanol, (R)- 1-methyl-2-(2,2-dimethyl-1,3-benzodioxol-5-yl)ethyl p-toluenesulfonate!, (R)- 1-methyl-2-(2,2-dimethyl-1,3-benzodioxol-5-yl)ethyl methanesulfonate!, (R)-2-chloro-1-(2,2-dimethyl-1,3-benzodioxol-5-yl)propane, (R)-2-bromo-1-(2,2-dimethyl-1,3-benzodioxol-5-yl)propane, etc.

As examples of the (4) (R)-1- 2,2-bis(C₂₋₅ alkoxycarbonyl)-1,3-benzodioxol-5-yl!-2-substituted propane derivative, there may be mentioned (R)- dimethyl 5-(2-hydroxypropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (R)- diethyl 5-(2-hydroxypropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (R)- dimethyl 5- 2-(p-toluenesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (R)- diethyl 5- 2-(p-toluenesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (R)- dimethyl 5- 2-(methanesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (R)- diethyl 5- 2-(methanesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (R)- dimethyl 5-(2-chloropropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (R)- diethyl 5-(2-chloropropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (R)- dimethyl 5-(2-bromopropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (R)- diethyl 5-(2-bromopropyl)-1,3-benzodioxole-2,2-dicarboxylate! and the like.

Examples of the (5) (R)-1-(2,2-dicarboxy-1,3-benzodioxol-5-yl)-2-substituted propane derivative include (R)- disodium 5- 2-(hydroxypropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (R)- disodium 5- 2-(p-toluenesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (R)- disodium 5- 2-(methanesulfonyloxy)propyl!-1,3-benzodioxole-2,2-dicarboxylate!, (R)- disodium 5-(2-chloropropyl)-1,3-benzodioxole-2,2-dicarboxylate!, (R)- disodium 5-(2-bromopropyl)-1,3-benzodioxole-2,2-dicarboxylate! and others.

The (R)-1-phenyl-2-substituted propane derivative of the general formula (VII) can be prepared by a variety of methods, for example, those mentioned in the (S)-1-phenyl-2-substituted derivative of the general formula (I) can be referred, and the object compound of the formula (VII) can advantageously be produced with the use of an action of a microorganism or a preparation thereof.

For example, the (R)-1-phenyl-2-substituted propane derivative shown by the general formula (VII) where X is a hydroxyl group, that is the compound of the formula (VII'), can readily be obtained by permitting a microorganism or a preparation thereof to act on the phenylacetone derivative of the general formula (II) to asymmetrically reduce and harvesting or recovering the product optically active (R)-1-phenyl-2-substituted propane derivative.

Any strain of microorganism that is capable of asymmetrically reducing the phenylacetone derivative of the general formula (II) to produce the optically active (R)-1-phenyl-2-substituted propanol derivative (VII') can be used in the method.

Examples of such microorganism include a strain of microorganisms belonging to the genus Corynebacterium, the genus Xanthomonas, the genus Micrococcus, the genus Botryoascus and the genus Candida.

(75) The strain of microorganism belonging to the genus Corynebacterium includes Corynebacterium variabilis JCM 2154, etc.

(76) The strain of microorganism belonging to the genus Xanthomonas includes Xanthomonas sp. IFO 3085, etc.

(77) The strain of microorganism belonging to the genus Micrococcus includes Micrococcus luteus AHU 1427, etc.

(78) The strain of microorganism belonging to the genus Botryoascus includes Botryoascus synaedendrus IFO 1604, etc.

(79) The strain of microorganism belonging to the genus Candida includes Candida parapsilosis IFO 0585, etc.

For producing the optically active (R)-1-phenyl-2-substituted propane derivative of the formula (VII), any of wild strains, mutants and recombinant strains which can be obtained by a genetic engineering technique such as cell fusion or gene manipulation can preferably be employed, as far as having the above mentioned ability or capability.

The strains of microorganisms each designated by IFO, JCM or AHU numbers can be available from the above-identified organizations.

The cultivation of the microorganism, asymmetric reduction and recovery of the reaction product can be conducted by similar manners as in the production of the (S)-1-phenyl-2-substituted propane derivative of the general formula (III).

In the (R)-1-phenyl-2-substituted propane derivative of the general formula (VII), R¹ and R² can be converted from one substituent to another by a conventional manner similarly in the compound (I).

The (R)-1-phenyl-2-substituted propane derivative of the formula (VII) may be converted to the (S)-1-phenyl-2-substituted propane derivative of the formula (I) by, for example, subjecting the (R)-enantiomer to nucleophilic substitution reaction accompanied with a steric inversion. Such reaction can be conducted with the use of a nucleophilic reagent for introducing X or a group convertible to X to produce a sterically inverted (S)-enantiomer.

The (R)-1-phenyl-2-substituted propane derivative where X is a hydroxyl group, that is, the compound of the general formula (VII') can easily be converted to the (S)-1-phenyl-2-substituted propane derivative of the general formula (I) wherein X is a hydroxyl group or a halogen atom, namely, the compound shown by the general formula (VIII) by selecting an reagent, a catalyst and reaction conditions from a suitable range wherein the reaction is proceeded with steric inversion. For example, the reaction can be carried out in accordance with the following scheme: ##STR11##

In the general formula (VIII), X¹ represents a hydroxyl group or a halogen atom. The halogen atom includes halogen atoms as mentioned above.

The conversion of the compound of the general formula (VII') to the compound of the general formula (VIII) wherein X¹ is a hydroxyl group can be carried out by, for example, the following method according to Mitsunobu reaction.

The (S)-1-phenyl-2-substituted propane derivative of the general formula (VIII) wherein X¹ is a hydroxyl group can be obtained by allowing an organic acid to react with the compound of the general formula (VII') in the presence of triarylphosphine (e.g. triphenylphosphine, etc.) and an azodicarboxylic acid ester such as ethyl azodicarbonate to form the sterically inverted corresponding organic acid ester, and hydrolyzing the resulting ester. The organic acid includes, for example, formic acid, acetic acid, trichloroacetic acid, trifluoroacetic acid, benzoic acid and the like. The formation of the organic acid ester may be conducted, for example, at a temperature of about -60° C. to 60° C. The reaction may be carried out in an inert solvent such as an aromatic hydrocarbon (for example, benzene, toluene and so on) and an ether (e.g. tetrahydrofuran, etc.). The proportions of triarylphosphine, organic acid and azodicarboxylic acid ester based on 1 mole of the compound of the general formula (VII') are respectively about 0.7 to 2.0 moles. The hydrolysis of the organic acid ester can be conducted by a conventional manner such as acid-hydrolysis or alkali-hydrolysis.

Such method utilizing Mitsunobu reaction wherein an optically active alcohol is sterically inverted to the corresponding optically active alcohol may refer to methods or those analogous thereto described, for example, in Synthesis, 1 (1981); Tetrahedron Lett., 1619 (1973); and Bull. Chem. Soc. Jpn., 44, 3427 (1971), and these descriptions can be incorporated to the present specification.

For the conversion of the optically active alcohol to the corresponding enantiomer, following methods can also be applied:

(a) the method comprising esterifying an optically active alcohol to a carboxylic acid ester such as trichloroactic acid ester, and hydrolyzing the resultant carboxylic acid ester, in a water-ether solvent such as 75% H₂ O-dioxane, can also be applied (see Chem. Lett., 1976, 893), and

(b) the method which comprises (a) converting an optically active alcohol to a sulfonic acid ester such as p-toluenesulfonic acid ester, (b) allowing an organic acid salt such as tetraethylammonium acetate and sodium acetate (-acetic acid) to react with the resulting sulfonic acid ester to sterically invert to the corresponding organic acid ester, and (c) hydrolyzing the resultant organic acid ester (J. Am. Chem. Soc., 87, 3682, (1965); and J. Chem. Soc., 1954, 965).

The (S)-1-phenyl-2-substituted propane derivative of the general formula (VIII) wherein X¹ is a halogen atom can be prepared from the compound of the formula (VII') by choosing a reagent, a catalyst, a solvent, and other reaction conditions from an adequate range as far as the reaction may be conducted with sterically inverting.

The conversion of the compound of the general formula (VII') to the compound of the general formula (VIII) wherein X¹ is a halogen atom can be carried out, for example, by the following procedure (J. Chem. Soc., 1709 (1953); and J. Chem. Soc., 3795 (1954)).

The reaction can be carried out by allowing a halogenating agent such as phosphorus pentachloride, phosphorus pentabromide, thionyl chloride and thionyl bromide to react with the compound of the general formula (VII') in the presence of a base such as the inorganic base (e.g. calcium carbonate) and the organic base as mentioned above to invert the compound sterically. The halogenation may be carried out, for instance, at about -20° C. to 150° C. The reaction may be conducted in an inert solvent such as an aromatic hydrocarbon (for instance, benzene, toluene and the like) and a halogenated hydrocarbon (e.g. methylene chloride, chloroform and so on). Where thionyl chloride or thionyl bromide is employed, the reaction may frequently be carried out in the presence of a base as exemplified above, or an organic base may frequently be used as the solvent to improve the inversion rate. Examples of such organic base include amines such as triethylamine, N,N-dimethylaniline and N-methylpiperidine; and nitrogen-containing heterocyclic compounds such as pyridine and picoline.

The proportion of the halogenating agent relative to 1 gram equivalent of the (R)-1-phenyl-2-propanol derivative of the general formula (VII'), is, for example, about 0.9 gram equivalent or more, and preferably about 0.9 to 1.5 gram equivalents. A reaction accelerator such as sodium chloride, sodium bromide and N,N-dimethylformamide may be added to the reaction system in order to proceed the reaction steadily or smoothly.

For the conversion of the (R)-1-phenyl-2-substituted propane derivative of the general formula (VII') to the (S)-1-phenyl-2-substituted propane derivative of the general formula (I) where X is a halogen atom, the following descriptions in literatures can also be referred and incorporated into the present specification:

(1) the method allowing a methanesulfonyl halide (e.g. methanesulfonyl chloride) to react with an optically active alcohol in the presence of a base and lithium halide such as lithium chloride (J. Org. Chem., 56, 2769 (1991))

(2) the method comprising allowing a p-toluenesulfonyl halide (e.g. p-toluenesulfonyl chloride) to react with an optically active alcohol in the presence of a base to produce a p-toluenesulfonic acid ester and allowing the resultant ester to react with a tetraalkylammonium halide such as tetraalkylammonium chloride (Tetrahedron Lett., 3425 (1990)),

(3) the method allowing an N,N-dialkyl-1,2,2-trihalovinylamine (e.g. N,N-diethyl-1,2,2-trichlorovinylamine) to react with an optically active alcohol (J. Am. Chem. Soc., 82, 909 (1960)),

(4) the method where a tetraalkyl-α-halogenoenamine (for instance, tetramethyl-α-chloroenamine) to react with an optically active alcohol (Tetrahedron Lett., 30, 3077 (1989)),

(5) the method allowing gaseous hydrochloric acid to react with a mixture of an optically active alcohol and nitrile to convert a halogenated compound via an imidate (J. Am. Chem. Soc., 77, 2341 (1955); Ber. Deutsch Chem. Ges., 92, 370 (1959); and Tetrahedron Lett., 2517 (1970)),

(6) the method where a carbon tetrahalide such as carbon tetrachloride and carbon tetrabromide is allowed to react with an optically active alcohol in the presence of triphenylphosphine (J. Org. Chem., 56, 3009 (1991); and Chem. Ind (London), 1017 (1969)),

(7) the method allowing an azodicarboxylic acid ester such as ethyl azodicarbonate, and a methyl halide such as methyl bromide to react with an optically active alcohol in the presence of triphenylphosphine (Tetrahedron, 39, 2591 (1983)),

(8) the method allowing a zinc halide (e.g. zinc chloride), an azodicarboxylic acid ester (for instance, ethyl azodicarbonate) and triphenylphosphine to react with an optionally active alcohol (J. Org. Chem., 49, 3027 (1984); Tetrahedron Lett., 28, 4199 (1987); and Herb. Chem. Acta, 32, 184 (1949)),

(9) the method which comprises allowing a 2-dialkylamino N,N'-diphenyl-1,3,2-diazaphosphorane such as 2-dimethylamino N,N'-diphenyl-1,3,2-diazaphosphorane to react with an optically active alcohol to produce a corresponding 2-alkoxy N,N'-diphenyl-1,3,2-diazaphosphorane and allowing a halogenating agent (e.g. sulfuryl chloride, bromine, methyl iodide, etc.) to react with the resulting compound (Tetrahedron Lett., 23, 4411 (1982)), and

(10) the method where 3-alkyl-2-fluorobenzothiazolium tetrafluoroborate such as 3-ethyl-2-fluorobenzothiazolium tetrafluoroborate to react with an optically active alcohol in the presence of a metal halide such as sodium chloride, sodium bromide, sodium iodide, lithium chloride, lithium bromide and lithium iodide (Chem. Lett., 619 (1976)).

The obtained (S)-1-phenyl-2-substituted propane derivative of the general formula (VIII) is an specifically important intermediate for production of the (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative. Accordingly, the (R)-1-phenyl-2-substituted propane derivative of the general formula (VII) of the present invention is remarkably usable as an intermediate material for the (S)-1-phenyl-2-substituted propane derivative.

The methods for conversion of the (R)-1-phenyl-2-substituted propane derivative of the general formula (VII) to the (S)-1-phenyl-2-substituted propane derivative of the general formula (I) can also be applied to the conversion of the corresponding (S)-enantiomer to the (R)-enantiomer.

The following examples are intended to illustrate the invention in further detail and should by no means be construed as delimiting the scope of the invention.

EXAMPLES

The quantitative determination and optical purity determination of 1-(3,4-dimethoxyphenyl)-2-propanol in the reaction mixture were carried out by subjecting the reaction mixture to high performance liquid chromatography using an optical resolution column (column: Chiralcel OF (trade name), Daicel Chemical Industries, Ltd.; solvent: n-hexane/2-propanol=90/10; flow rate: 1 ml/min.; temperature: 40° C.; wavelength: 220 nm).

Examples 1 to 139

Production of (S)-1-(3,4-dimethoxyphenyl)-2-propanol

YM Medium (0.3% by weight of yeast extract, 0.3% by weight of malt extract, 0.5% by weight of peptone, 2% by weight of glucose, pH 6.0) was used for strains of microorganism belonging to yeasts, and PM medium (2% by weight of glucose, 0.3% by weight of peptone, 0.5% by weight of yeast extract, 0.3% by weight of meat extract, 0.2% by weight of ammonium sulfate, 0.1% by weight of potassium dihydrogenphosphate, 0.05% by weight of magnesium sulfate, pH 7.0) was used for strains of microorganism belonging to bacteria.

A test tube of diameter of 21 mm was charged with 5 ml of the above mentioned medium respectively. After sterilization, the tube was inoculated with one of the following microbial strains. The inoculated tube was incubated under shaking at 30° C. for 24 hours.

Example 1

Sphingobacterium sp. IFO 13310

Example 2

Aeromonas hydrophila subsp. proteolytiga IFO 13287

Example 3

Agrobacterium radiobacter IFO 12664

Example 4

Aureobacterium testaceum IFO 12675

Example 5

Bacillus cereus AHU 1355

Example 6

Cellulomonas flavigena IFO 3754

Example 7

Chromobacterium iodinum IFO 3558

Example 8

Corynebacterium aquaticum IFO 12154

Example 9

Gluconobacter oxydans IFO 3255

Example 10

Jensenia canicruria IFO 13914

Example 11

Comamonas acidovorans IFO 13582

Example 12

Pseudomonas fluorescens IFO 3081

Example 13

Pseudomonas putida IFO 3738

Example 14

Alternaria japonica IFO 5244

Example 15

Amanita citrina IFO 8261

Example 16

Aspergillus awamori nakazawa IFO 4033

Example 17

Aspergillus ficuum IFO 4018

Example 18

Aspergillus niger AHU 7105

Example 19

Aspergillus niger IFO 5374

Example 20

Cochliobolus miyabeanus IFO 6631

Example 21

Corynespora cassiicola IFO 6724

Example 22

Dactylium dendroides ATCC 46032

Example 23

Drechslera avenae IFO 6636

Example 24

Echinopodospora jamaicensis IFO 9819

Example 25

Gelasinospora cerealis IFO 6759

Example 26

Gonatobotryum apiculatum IFO 9098

Example 27

Helminthosporium sigmoideum var. irregulare IFO 5273

Example 28

Mortierella isabeilina IFO 6336

Example 29

Paecilomyces variotii IFO 4855

Example 30

Phialophora pedrosoi IFO 6071

Example 31

Phytophthora capsici IFO 8386

Example 32

Podospora carbonaria IFO 30294

Example 33

Rhizomucor pusillus IFO 4578

Example 34

Septoria glycines IFO 5294

Example 35

Sporormielia isomera IFO 8538

Example 36

Stemphylium sarciniforme IFO 7243

Example 37

Talaromyces flavus var. flavus IFO 7231

Example 38

Torula jeanselmei IFO 6857

Example 39

Ustilago cynodontis IFO 7530

Example 40

Westerdykella multispora IFO 5813

Example 41

Ambrosiozyma cicatricosa IFO 1846

Example 42

Ambrosiozyma monospora IFO 1965

Example 43

Dekkera custersianus IFO 1585

Example 44

Candida aaseri IFO 10104

Example 45

Candida atomspherica IFO 1969

Example 46

Candida beechii IFO 10229

Example 47

Candida diversa IFO 1091

Example 48

Candida ergatensis IFO 10233

Example 49

Candida fluviatilis IFO 10234

Example 50

Candida fusiformate IFO 10225

Example 51

Candida glabrata IFO 0622

Example 52

Candida gropengiesseri IFO 0659

Example 53

Candida halonitratophila IFO 1595

Example 54

Candida inconspicua IFO 0621

Example 55

Candida kefyr DSM 70073

Example 56

Candida krusei DSM 70075

Example 57

Candida lambica DSM 70090

Example 58

Candida mogii IFO 0436

Example 59

Candida maltosa IFO 1978

Example 60

Candida melibiosica IFO 10238

Example 61

Candida membranaefaciens IFO 1246

Example 62

Candida oleophila JCM 2444

Example 63

Candida parapsilosis IFO 1022

Example 64

Candida pintolopesii var. pintolopesii IFO 0729

Example 65

Candida pseudointermedia IFO 1693

Example 66

Candida catenulata DSM 70136

Example 67

Candida rugosa IFO 0591

Example 68

Candida saitoana IFO 0768

Example 69

Candida sake IFO 1149

Example 70

Candida natalensis IFO 1981

Example 71

Candida salmanticensis IFO 10242

Example 72

Candida santamariae IFO 1982

Example 73

Candida schatavii IFO 10258

Example 74

Candida shehatae IFO 1983

Example 75

Candida silvanorum IFO 10419

Example 76

Candida sorbophila IFO 1583

Example 77

Candida tenuis IFO 10315

Example 78

Candida utilis IFO 0396

Example 79

Candida utilis IFO 0988

Example 80

Candida albicans IFO 0759

Example 81

Clavispora lusitaniae IFO 1019

Example 82

Cryptococcus humicolus IFO 0760

Example 83

Cryptococcus neoformans IAM 4788

Example 84

Debaryomyces varijiae DSM 70252

Example 85

Galactomyces reessii IFO 1112

Example 86

Filobasidium capsuligenum IFO 1119

Example 87

Geotrichum candidum IFO 4598

Example 88

Geotrichum fermentans JCM 2467

Example 89

Geotrichum fragrans JCM 2450

Example 90

Hansenula polymorpha ATCC 26012

Example 91

Hansenula capsulata DSM 70269

Example 92

Hansenula glucozyma DSM 70271

Example 93

Hansenula wickerhamii DSM 70280

Example 94

Issatchenkia scutulata var. scutulata IFO 10070

Example 95

Kloeckera africana IFO 0869

Example 96

Kluyveromyces lactis IFO 0433

Example 97

Kluyveromyces marxianus DSM 70800

Example 98

Kluyveromyces polysporus DSM 70294

Example 99

Leucosporidium scottii IFO 1924

Example 100

Lodderomyces elongisporus IFO 1676

Example 101

Metschnikowia bicuspidata IFO 1408

Example 102

Metschnikowia pulcherrima DSM 70336

Example 103

Metschnikowia reukaufii DSM 70880

Example 104

Myxozyma lipomycoides IFO 10350

Example 105

Oosporidium margaritiferum IFO 1208

Example 106

Pachysolen tannophilus IFO 1007

Example 107

Pichia cellobiosa DSM 2147

Example 108

Pichia farinosa IFO 1163

Example 109

Pichia lindnerii DSM 70718

Example 110

Pichia ohmeri DSM 70815

Example 111

Pichia thermotolerans IFO 10025

Example 112

Pichia pastoris DSM 70382

Example 113

Pichia trehalophila DSM 70391

Example 114

Pichia carsonii DSM 70392

Example 115

Pichia subpelliculosa IFO 0808

Example 116

Malassezia furfur IFO 0656

Example 117

Rhodosporidium diobovatum IFO 1830

Example 118

Rhodosporidium toruloides IFO 1638

Example 119

Kondoa malvinella IFO 1936

Example 120

Rhodotorula glutinis AHU 3454

Example 121

Rhodotorula rubra IFO 0383

Example 122

Saccharomyces rouxii IAM 0487

Example 123

Octosporomyces octosporus IFO 0353

Example 124

Sporidiobolus johnsonii IFO 6903

Example 125

Sporidiobolus pararoseus IFO 1104

Example 126

Sporidiobolus salmonicolor IFO 1845

Example 127

Sporobolomyces pararoseus IFO 1036

Example 128

Sporopachydermia lactativora IFO 1867

Example 129

Sterigmatomyces elviae DSM 70852

Example 130

Torulaspora delbrueckii IFO 0381

Example 131

Torulopsis nemodendra DSM 70647

Example 132

Trigonopsis variabilis IFO 0755

Example 133

Wickerhamia fluorescens DSM 70715

Example 134

Wickerhamiella domercquii IFO 1857

Example 135

Wingea robertsii IFO 1277

Example 136

Zygoascus hellenicus IFO 1575

Example 137

Zygosaccharomyces bailii IFO 0468

Example 138

Zygosaccharomyces bisporus DSM 70415

Example 139

Zygozyma oligophaga IFO 10360

The cells were isolated by centrifuging and suspended in 1 ml of 0.1M phosphate buffer (pH 7.0) containing 0.5% by weight of 3,4-dimethoxyphenylacetone and 5% by weight of glucose. A test tube of 21 mm diameter was charged with the suspension and reaction was conducted on a reciprocating shaker at 30° C. for 48 hours.

After completion of the reaction, the reaction suspension was added with a small amount of sodium chloride and extracted with 5 ml of n-hexane. The n-hexane extract was subjected to determination and the optical purity and the yield of the product 1-(3,4-dimethoxyphenyl)-2-propanol were determined. The results are set forth in Tables 1 to 7.

                  TABLE 1     ______________________________________                  (S)-1-(3,4-dimethoxy-                  phenyl)-2-propanol     Example        Yield  Optical purity     No.            (%)    (% e.e.)     ______________________________________      1             39.5   29.1      2             29.2   94.6      3             10.9   91.8      4             42.0   94.3      5             18.8   92.7      6             16.2   77.2      7             11.7   23.0      8             43.0   47.9      9             20.3   98.6     10             22.4   92.3     11             10.3   90.2     12             14.1   77.0     13             10.0   94.5     14             10.8   80.9     15             12.4   85.6     16             13.8   79.8     17             10.0   98.6     18             15.0   83.3     19             15.2   80.4     20             15.6   67.3     ______________________________________

                  TABLE 2     ______________________________________                  (S)-1-(3,4-dimethoxy-                  phenyl)-2-propanol     Example        Yield  Optical purity     No.            (%)    (% e.e.)     ______________________________________     21             11.2   88.9     22             13.8   92.4     23             11.0   95.8     24             21.0   98.0     25             26.0   94.4     26             13.8   67.0     27             14.8   98.3     28             17.2   96.2     29             32.0   93.9     30             11.4   84.9     31             28.4   96.7     32             10.6   82.4     33             15.0   92.0     34             12.8   91.0     35             12.8   64.2     36             13.2   69.7     37             15.0   93.9     38             26.4   25.9     39             11.8   94.7     40             18.2   72.2     ______________________________________

                  TABLE 3     ______________________________________                  (S)-1-(3,4-dimethoxy-                  phenyl)-2-propanol     Example        Yield  Optical purity     No.            (%)    (% e.e.)     ______________________________________     41             28.4   98.8     42             22.2   97.0     43             12.2   95.6     44             43.4   97.7     45             24.6   93.8     46             19.0   92.0     47             14.9   66.2     48             37.5   38.3     49             34.3   69.4     50             15.4   79.0     51             18.5   93.3     52             21.4   66.7     53             15.8   76.9     54             10.6   77.5     55             35.2   99.2     56             17.2   66.2     57             47.1   98.6     58             19.2   80.2     59             21.9   19.1     60             15.7   96.2     ______________________________________

                  TABLE 4     ______________________________________                  (S)-1-(3,4-dimethoxy-                  phenyl)-2-propanol     Example        Yield  Optical purity     No.            (%)    (% e.e.)     ______________________________________     61             40.8   81.6     62             25.2   76.4     63             22.4   85.0     64             10.7   84.2     65             10.7   57.0     66             10.3   89.3     67             21.6   89.3     68             21.5   98.2     69             69.1   96.9     70             12.9   20.6     71             10.5   79.5     72             38.6   84.9     73             23.6   83.0     74             18.4   83.0     75             37.7   92.3     76             10.4   83.6     77             10.1   65.3     78             26.3   96.9     79             42.9   97.6     80             34.2   87.0     ______________________________________

                  TABLE 5     ______________________________________                  (S)-1-(3,4-dimethoxy-                  phenyl)-2-propanol     Example        Yield  Optical purity     No.            (%)    (% e.e.)     ______________________________________     81             69.5   94.2     82             16.7   77.8     83             13.8   97.2     84             25.5   98.3     85             24.1   99.2     86             29.8   99.1     87             12.3   99.4     88             18.0   95.0     89             17.5   98.2     90             66.1   97.3     91             34.0   99.0     92             44.7   86.6     93             25.8   76.5     94             10.2   75.5     95             14.8   53.0     96             27.9   96.4     97             40.9   93.0     98             22.1   92.2     99             35.0   95.9     100            33.8   62.1     ______________________________________

                  TABLE 6     ______________________________________                  (S)-1-(3,4-dimethoxy-                  phenyl)-2-propanol     Example        Yield  Optical purity     No.            (%)    (% e.e.)     ______________________________________     101            39.6   79.4     102            25.6   90.9     103            13.1   78.6     104            38.4   99.0     105            14.8   52.9     106            24.6   96.3     107            15.4   78.6     108            34.9   92.8     109            71.3   97.9     110            17.0   76.9     111            16.9   97.4     112            71.3   97.9     113            28.2   97.8     114            19.3   90.1     115            13.3   98.5     116            13.9   78.2     117            29.9   96.4     118            86.3   98.4     119            23.7   77.0     120            10.4   96.8     ______________________________________

                  TABLE 7     ______________________________________                  (S)-1-(3,4-dimethoxy-                  phenyl)-2-propanol     Example        Yield  Optical purity     No.            (%)    (% e.e.)     ______________________________________     121            24.0   73.9     122            33.0   97.7     123            58.8   69.2     124            64.4   97.4     125            12.6   94.8     126            18.3   94.3     127            19.9   95.2     128            38.4   99.0     129            26.7   78.0     130            57.1   98.3     131            10.0   85.3     132            11.3   85.9     133            27.9   100     134            16.4   92.3     135            10.4   95.2     136            34.2   94.8     137            11.5   93.9     138            23.4   93.2     139            32.6   96.3     ______________________________________

Example 140

Production of (S)-1-(3,4dimethoxyphenyl)-2-propanol

A 2.6-liter mini jar fermenter was charged with 1.5 liter of YM media of the same composition as mentioned in Examples 1 to 139. After sterilization with the use of an autoclave, the fermenter was inoculated with Torulaspora delbrueckii IFO 0381, and the inoculated fermenter was incubated at 30° C., under aeration at 1 vvm, with stirring at 400 rpm for 24 hours. After completion of incubation, the cells were concentrated by centrifuging.

A 2.6-liter mini far fermenter was charged with 1 liter of 0.1M phosphate buffer (pH 7.0) and the obtained cells were suspended therein. To the suspension was added 5 g of 3,4-dimethoxyphenylacetone and 50 g of glucose, and the reaction was carried out at 30° C., under aeration at 1 vvm, with stirring at 400 rpm for 48 hours.

After completion of the reaction, the cells were removed off by centrifuging, and the obtained supernatant was added with 400 g of sodium chloride, and extracted with 1 liter of ethyl acetate three times. The ethyl acetate extract was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure to give 3.1 g of an oily substance. The oily substance was purified with the use of silica gel chromatography (eluent: n-hexane/ethyl acetate=7/3) to give 2.7 g of crystalline (S)-1-(3,4-dimethoxyphenyl)-2-propanol (m.p.: 51° C.). The specific rotation of the compound was α!_(D) ²⁰ +28.3° (c=1.06, chloroform). As a result of analyzing the compound by high performance liquid chromatography using an optical resolution column (column: Chiralcel OF (trade name), Daicel Chemical Industries, Ltd.), the optical purity thereof was 100% e.e.

¹ H-NMR (270 MHz, CDCl₃) δ: 1.24 (d, 3H), 1.72 (br, s, 1H), 2.66 (m, 2H), 3.86 (d, 6H), 3.99 (m, 1H), 6.76 (m, 3H)

IR (cm⁻¹): 3400, 2880, 1515, 1460, 1260, 1240, 800

The absolute configuration of the obtained 1-(3,4-dimethoxyphenyl)-2-propanol was determined by the following manner.

The 1-(3,4-dimethoxyphenyl)-2-propanol obtained above was subjected to sulfonylation by p-toluenesulfonyl chloride and reacted with benzylamine to give N-benzyl-3,4-dimethoxyamphetamine. The resultant compound was converted into 3,4-dimethoxyamphetamine by hydrogenation decomposition under hydrogen atmosphere with 5% Pd-C.

As a result of the determination of the obtained 3,4-dimethoxyamphetamine, the specific rotation thereof was α!_(D) ²⁵ -26.5° (c=4.58, chloroform).

To an ethanol solution of the 3,4-dimethoxyamphetamine was added an equivalent amount of (half time as much mole of) concentrated sulfuric acid to yield 3,4-dimethoxyamphetamine.1/2H₂ SO₄ as crystals. The specific rotation of the sulfuric acid salt was α!_(D) ²⁵ -19.03° (c=2.27, H₂ O). The obtained 3,4-dimethoxyamphetamine was determined as an (R)-form since the values in a literature (J. Org. Chem., 22, 33 (1957)) are as follows.

(R)-3,4-dimethoxyamphetamine:

α!_(D) -30.9° (c=4.13, chloroform)

(R)-3,4-dimethoxyamphetamine.1/2H₂ SO₄ :

α!_(D) -21.4° (c=2.0, H₂ O)

Since the reaction where 3,4-dimethoxyamphetamine is produced from 1-(3,4-dimethoxyphenyl)-2-propanol is accompanied by inversion, the 1-(3,4-dimethoxyphenyl)-2-propanol obtained above was proved to be an (S)-enantiomer.

Example 141

Production of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl p-toluenesulfonate

To a solution of 404 mg of (S)-1-(3,4-dimethoxyphenyl)-2-propanol in 2 ml of pyridine was added 472 mg of p-toluenesulfonyl chloride under nitrogen atmosphere on an ice bath. The mixture was stirred at 20° C. for 17 hours. Granules of ice were added to the mixture to cease the reaction, and the reaction mixture was stirred for further 30 minutes. The reaction mixture was acidified by adding 2N hydrochloric acid and was extracted twice with 20 ml of chloroform. The organic extract was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, distilled off the solvent to give 716 mg of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl p-toluenesulfonate! as white crystals (yield: 98%). Analysis of the compound by high performance liquid chromatography using an optical resolution column (column: Chiralcel OF (trade name), Daicel Chemical Industries, Ltd.) revealed that the optical purity thereof was 100% e.e.

m.p.: 62.4 to 62.8° C. α!_(D) ²⁵ +20.6° (c=1.0, chloroform)

IR (KBr) (cm⁻¹): 3044, 2995, 2937, 1594, 1517, 1357, 1346, 1262, 1243, 1187, 1178, 1169, 1157, 1142, 1029, 913, 889, 854, 806, 766, 666, 578, 558

¹ H-NMR (500 MHz, CDCl₃) δ: 1.34 (d, 3H), 2.41 (s, 3H), 2.73 (dd, 1H), 2.83 (dd, 1H), 3.76 (s, 3H), 3.86 (s, 3H), 4.70 (m, 1H), 6.47 (d, 1H), 6.59 (m, 1H), 6.69 (d, 1H), 7.24 (d, 2H), 7.57 (d, 2H)

¹³ C-NMR (125 MHz, CDCl₃) δ: 20.74, 21.49, 42.48, 55.54, 55.76, 80.88, 110.90, 112.21, 121.44, 127.48, 128.80, 129.41, 133.48, 144.19, 147.81, 148.61

Example 142

Production of (R,R)-1-(³ -chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

(R)-2-Amino-1-(3-chlorophenyl)ethanol (806 mg) was added to (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl p-toluenesulfonate! (700 mg) under nitrogen atmosphere, and the mixture was stirred at 60° C. for 31 hours. The reaction mixture was adjusted to alkaline by adding a 10% aqueous solution of sodium hydroxide, and extracted twice with 20 ml of chloroform. The organic extract was dried over anhydrous sodium sulfate, subjected to distilling off the solvent and to purifying with silica gel chromatography (eluent: chloroform/methanol) to give 550 mg of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol as white crystals (yield: 79%). The NMR spectrum data are shown as follows.

¹ H-NMR (500 MHz, CDCl₃) δ: 1.09 (d, 3H), 2.08 (brs, 2H), 2.61-2.69 (m, 3H), 2.87-2.92 (m, 2H), 3.86 (s, 3H), 3.87 (s, 3H), 4.55 (dd, 1H), 6.68 (s, 1H), 6.70 (d, 1H), 6.80 (d, 1H), 7.18-7.26 (m, 3H), 7.35 (s, 1H)

¹³ C-NMR (125 MHz, CDCl₃) δ: 20.37, 43.39, 54.09, 54.26, 55.87, 55.89, 71.11, 111.21, 112.36, 121.19, 123.89, 125.94, 127.55, 129.61, 131.56, 134.32, 144.66, 147.57, 148.87

The optical purity of the compound was determined by converting the compound into a corresponding cyclic urethane derivative. That is, the compound was converted into (R,R)-5-(3-chlorophenyl)-3- 2-(3,4-dimethoxyphenyl)-1-methylethyl!-2-oxazolidinone by allowing carbonyldiimidazole and N-methylmorpholine to react with the compound in tetrahydrofuran at room temperature for 2 hours, then heating the mixture under reflux for 3 hours. Analyzing the compound by high performance liquid chromatography using an optical resolution column (column: Chiralcel AS (trade name), Daicel Chemical Industries, Ltd.), the optical purity of the compound was 90% e.e. The NMR spectrum data of the obtained cyclic urethane derivative are set forth hereinbelow.

¹ H-NMR (500 MHz, CDCl₃) δ: 1.26 (d, 3H), 2.67 (dd, 1H), 2.81 (dd, 1H), 3.24 (dd, 1H), 3.81 (s, 3H), 3.83 (dd, 1H), 3.86 (s, 3H), 4.33 (ddq, 1H), 5.35 (dd, 1H), 6.63 (d, 1H), 6.70 (s, 1H), 6.73 (d, 1H), 6.91 (d, 1H), 7.12 (s, 1H), 7.22 (dd, 1H), 7.28 (d, 1H)

¹³ C-NMR (125 MHz, CDCl₃) δ: 17.72, 39.71, 47.69, 49.55, 55.75, 55.79, 73.38, 111.03, 111.75, 120.76, 123.44, 125.56, 128.73, 129.76, 130.07, 134.62, 141.14, 147.71, 148.90, 156.90

Examples 143 to 147

Production of (R)-1-(3,4-dimethoxyphenyl)-2-propanol

The cultivating procedures and reaction procedures were conducted in the same manner as in Examples 1 to 139 except for using the following strains of microorganisms. The results are shown in Table 8.

Example 143

Corynebacterium variabilis JCM 2154

Example 144

Xanthomonas sp. IFO 3085

Example 145

Micrococcus luteus AHU 1427

Example 146

Botryoascus synaedendrus IFO 1604

Example 147

Candida parapsilosis IFO 0585

                  TABLE 8     ______________________________________                  (R)-1-(3,4-dimethoxy-                  phenyl)-2-propanol     Example        Yield  Optical purity     No.            (%)    (% e.e.)     ______________________________________     143            12.6   74.9     144            18.6   83.9     145            19.3   53.2     146            20.6   34.5     147            31.1   10.6     ______________________________________

Example 148

Production of (S)-1-(3,4-dimethoxyphenyl)-2-propanol

(R)-1-(3,4-Dimethoxyphenyl)-2-propanol (0.9 g) was obtained as crystals by cultivation, reaction and purification in the similar manners as in Example 140 except that PM medium was employed instead of YM media and that Xanthomonas sp. IFO 3085 was used instead of Torlaspora delbrueckii IFO 0381. The crystals gave the same signals in ¹ H-NMR analysis as in the (S)-1-(3,4-dimethoxyphenyl)-2-propanol obtained in Example 140. Further the specific rotation of the crystals was "-", therefore, the crystals were proved to be (R)-1-(3,4-dimethoxyphenyl)-2-propanol. As a result of determination by high performance liquid chromatography with the use of a optical resolution column, the optical purity of the compound was 85.5% e.e.

Thus obtained (R)-1-(3,4-dimethoxyphenyl)-2-propanol (744 mg, 3.80 mmol.), triphenylphosphine (1196 mg) and formic acid (210 mg) were dissolved in 60 ml of tetrahydrofuran, and to the resultant solution, was added a solution of 794 mg of diethyl azodicarbonate in 10 ml of tetrahydrofuran. The mixture was stirred at room temperature for 15 hours, and reaction mixture was concentrated under reduced pressure. The resulting residue was subjected to purification by silica gel chromatography (eluent: n-hexane/ethyl acetate=7/3) to give 595 mg of formic acid ester of (S)-1-(3,4-dimethoxyphenyl)-2-propanol. The ester was subjected to alkali-hydrolysis according to a known method and extracted with ethyl acetate, and the solvent was distilled off. The residue was purified by silica gel chromatography (eluent: n-hexane/ethyl acetate=7/3) to give 450 mg of (S)-1-(3,4-dimethoxyphenyl)-2-propanol as crystals. The optical purity of the compound was 99% e.e. by analyzing by high performance liquid chromatography with the use of an optical resolution column.

Example 149

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

A mixture of 57.0 g (0.163 mol) of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl p-toluenesulfonate!, 33.7 g (0.196 mol) of (R)-2-amino-1-(3-chlorophenyl)ethanol, 33.7 g (0.244 mol) of anhydrous potassium carbonate and 133 ml of toluene was stirred at 90° C. for 48 hours under nitrogen atmosphere. The reaction mixture was adjusted to alkaline by adding a 10% aqueous solution of sodium hydroxide and extracted twice with 500 ml of toluene. The toluene extract was dried over anhydrous sodium sulfate, and subjected to distillation of the solvent and to purification with silica gel chromatography to give 34.8 g of 1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol as white crystals (yield: 61%). As a result of isolating and analyzing the isomers with high performance liquid chromatography using an optical resolution column (column: Chiralpack AD (trade name), Daicel Chemical Industries, Ltd.), the optical purity of the title compound was 86.8% (R,R)/(R,S)=86.8/13.2!.

Example 150

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

Under nitrogen atmosphere, a mixture of 4.20 g (0.0120 mol) of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl p-toluenesulfonate!, 2.47 g (0.0144 mol) of (R)-2-amino-1-(3-chlorophenyl)ethanol and 1.82 g (0.0180 mol) of diisopropylamine was stirred at 60° C. for 48 hours. The reaction mixture was adjusted to alkaline by adding a 10% aqueous solution of sodium hydroxide and extracted twice with 500 ml of toluene. The toluene extract was dried over anhydrous sodium sulfate, and subjected to distillation of the solvent and to purification with silica gel chromatography to give 3.23 g of 1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol as white crystals (yield: 77%). As a result of isolation and analysis of the isomers by high performance liquid chromatography using an optical resolution column (column: Chiralpack AD (trade name), Daicel Chemical Industries, Ltd.), the optical purity of the objective compound was 92.8% (R,R)/(R,S)=92.8/7.2!.

Example 151

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

To 2.5 ml of toluene, were added 701 mg (2.00 mmol) of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl p-toluenesulfonate!, 412 mg (2.40 mmol) of (R)-2-amino-1-(3-chlorophenyl)ethanol and 207 mg (1.50 mmol) of anhydrous potassium carbonate, and the mixture was stirred at 90° C. for 24 hours under nitrogen atmosphere. After adjusted to alkaline by adding a 10% aqueous solution of sodium hydroxide, the reaction mixture was extracted twice with 30 ml of toluene. The toluene extract was dried over anhydrous sodium sulfate and subjected to distillation of the solvent and to purification with silica gel chromatography to afford 313 mg of 1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol as white crystals (yield: 45%). As a result of isolating and analyzing the isomers with high performance liquid chromatography using an optical resolution column (column: Chiralpack AD (trade name), Daicel Chemical Industries, Ltd.), the optical purity of the title compound was 88.3% (R,R)/(R,S)=88.3/11.7!.

Example 152

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

The procedure of Example 151 was followed except for using 415 mg (3.00 mmol) of anhydrous potassium carbonate to give 431 mg of 1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol (yield: 62%). The optical purity of the title compound was 87.5% (R,R)/(R,S)=87.5/12.5!.

Examples 153 and 154

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

The procedure of Example 151 was repeated except that the reaction was conducted using the solvent at the reaction temperature shown in Table 9. The results are set forth in Table 9.

                  TABLE 9     ______________________________________                 Reaction          Optical                 temperature                           Yield   purity     Solvent     (° C.)                           (%)     (%)   (R,R)/(R,S)     ______________________________________     Ex. 153           n-Octane  90        54    88.3  88.3/11.7     Ex. 154           Acetonitrile                     60        32    74.1  74.1/25.9     ______________________________________

Examples 155 and 156

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

The title compound was prepared in the same manner as in Example 151 except that 5 ml of toluene was used and that the bases shown in Table 10 were used instead of anhydrous potassium carbonate. The results are set forth in Table 10.

                  TABLE 10     ______________________________________                              Optical                     Yield    purity  (R,R)/(R,S)     Base            (%)      (%)     (%)     ______________________________________     Ex. 155 Sodium ethoxide                         44       87.9  87.9/12.1     Ex. 156 Diisopropylamine                         65       74.6  74.6/25.4     ______________________________________

Example 157

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

Under nitrogen atmosphere, 350 mg (1.00 mmol) of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl p-toluenesulfonate! was added to 206 mg (1.20 mmol) of (R)-2-amino-1-(3-chlorophenyl)ethanol, and the mixture was stirred at 60° C. for 24 hours. The reaction mixture was added with a 10% aqueous solution of sodium hydroxide to be alkaline, and extracted twice with 30 ml of toluene. The toluene extract was dried over anhydrous sodium sulfate, and subjected to distillation of the solvent and to purification with silica gel chromatography to give 187 mg of 1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol as white crystals (yield: 54%). As a result of isolating and analyzing the isomers by high performance liquid chromatography using an optical resolution column (column: Chiralpack AD (trade name), Daicel Chemical Industries, Ltd.), the optical purity of the title compound was 95.2% (R,R)/(R,S)=95.2/4.8!.

Example 158

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

To 274 mg (1.00 mmol) of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl methanesulfonate! was added 206 mg (1.20 mmol) of (R)-2-amino-1-(3-chlorophenyl)ethanol, and the mixture was stirred at 60° C. for 24 hours. The reaction mixture was added with a 10% aqueous solution of sodium hydroxide to be alkaline, and extracted twice with 30 ml of toluene. The toluene extract was dried over anhydrous sodium sulfate, and subjected to distillation of the solvent and to purification with silica gel chromatography to give 161 mg of 1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol as white crystals (yield: 46%). As a result of isolating and analyzing the isomers by high performance liquid chromatography using an optical resolution column (column: Chiralpack AD (trade name), Daicel Chemical Industries, Ltd.), the optical purity of the title compound was 95.8% (R,R)/(R,S)=95.8/4.2!.

Example 159

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

The procedure of Example 158 was followed, except that 403 mg (2.35 mmol) of (R)-2-amino-1-(3-chlorophenyl)ethanol was used, to give 252 mg of 1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol (yield: 72%). The optical purity of the title compound was 96.4% (R,R)/(R,S)=96.4/3.6!.

Example 160

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

To 274 mg (1.00 mmol) of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl methanesulfonate! were added 206 mg (1.20 mmol) of (R)-2-amino-1-(3-chlorophenyl)ethanol and 194 mg (1.50 mmol) of dibutylamine, and the mixture was stirred at 60° C. for 24 hours under nitrogen atmosphere. The reaction mixture was added with a 10% aqueous solution of sodium hydroxide to be alkaline, and extracted twice with 30 ml of toluene. The toluene extract was dried over anhydrous sodium sulfate, and subjected to distillation of the solvent and to purification with silica gel chromatography to give 190 mg of 1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol as white crystals (yield: 54%). As a result of isolating and analyzing the isomers by high performance liquid chromatography using an optical resolution column (column: Chiralpack AD (trade name), Daicel Chemical Industries, Ltd.), the optical purity of the objective compound was 95.2% (R,R)/(R,S)=95.2/4.8!.

Examples 161 to 166

Production of (R,R)-1-(3-chlorophenyl)-2- 2-(3,4-dimethoxyphenyl)-1-methylethyl!amino!ethanol

The title compound was prepared in the same manner as in Example 160, except that the reaction was carried out using the base, instead of dibutylamine, at the reaction temperature set forth in Table 11. The results are shown in Table 11.

                  TABLE 11     ______________________________________                    Reaction         Optical                                           (R,R)/                    temperature                              Yield  purity                                           (R,S)     Base           (° C.)                              (%)    (%)   (%)     ______________________________________     Ex. 161           Dibutylamine 75        69   86.8  86.8/13.2     Ex. 162           Triethylamine                        60        47   96.9  96.9/3.1     Ex. 163           Pyridine     60        39   98.3  98.3/1.7     Ex. 164           2-Pipecoline 60        57   96.0  96.0/4.0     Ex. 165           N-           60        39   95.9  95.9/4.1           Methylmorpholine     Ex. 166           N,N-Dimethyl-                        60        44   95.3  95.3/4.7           ethanolamine     ______________________________________

Example 167

Production of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl methanesulfonate

Under nitrogen atmosphere, to a methylene chloride solution (20 ml) of 4.91 g (0.025 mol) of (S)-1-(3,4-dimethoxyphenyl)-2-propanol and 3.79 g (0.038 mol) of triethylamine, was added dropwise a methylene chloride solution (10 ml) of 3.43 g (0.030 mol) of methanesulfonyl chloride under cooling with an ice bath for 30 minutes. The fixture was stirred for one hour, and the reaction was ceased by addition of 2N hydrochloric acid. The reaction mixture was extracted twice with 50 ml of methylene chloride. The methylene chloride extract was washed with a saturated solution of sodium chloride, dried and subject ed to distillation of the solvent to give 6.6 5 g of (S)- 2-(3,4-dimethoxyphenyl)-1-methylethyl methanesulfonate! as crystals (yield: 97%). As a result of the analysis by high performance liquid chromatography using an optical resolution column (column: Chiralpack AS (trade name), Daicel Chemical Industries, Ltd.), the optical purity of the title compound was 100%.

m.p.: 79.5 to 80.3° C.

α!_(D) ²⁵ +26.5 (c=1.24, chloroform)

IR (KBr) (cm⁻¹): 3018, 2973, 2937, 2843, 1607, 1590, 1518, 1469, 1447, 1342, 1265, 1238, 1174, 1148, 1122, 1028, 984, 916, 883, 856, 828, 801, 765, 719, 636, 546, 530, 477

¹ H-NMR (500 MHz, CDCl₃) δ: 6.82 (d, 1H), 6.77 (dd, 1H), 6.75 (d, 1H), 4.89 (m, 1H), 3.88 (s, 3H), 3.86 (s, 3H), 2.94 (dd, 1H), 2.85 (dd, 1H), 2.60 (s, 3H), 1.45 (d, 3H) 

What is claimed is:
 1. A process for producing an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative which comprises:allowing an (R)-2-amino-1-phenylethanol derivative shown by the following formula ##STR12## wherein R⁶, R⁷, R⁸, R⁹ and R¹⁰ respectively represent a hydrogen atom, a lower alkyl group, a lower haloalkyl group, a lower alkoxy group, a nitro group or a halogen atom; and Z represents a hydrogen atom or a protective group for hydroxyl group, to react with an (S)-1-phenyl-2-substituted propane derivative shown by the following formula ##STR13## wherein R¹ and R² represent (a) the same or different, a hydrogen atom or a protective group for hydroxyl group, or (b) R¹ and R² may form an optionally substituted ring together with the adjacent oxygen atoms; R³, R⁴ and R⁵ independently represent a hydrogen atom, a lower alkyl group, a lower haloalkyl group, a lower alkoxy group, a nitro group or a halogen atom; and Y represents an optionally substituted alkylsulfonyloxy group, an optionally substituted arylsulfonyloxy group or a halogen atom, to produce an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative shown by the following formula ##STR14## wherein R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and Z have the same meanings as defined above, or a salt thereof.
 2. A process for producing an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative according to claim 1, wherein the reaction of the compound of the formula (V) and the compound of the formula (IV) is conducted in the presence of a base.
 3. A process for producing an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative according to claim 1, wherein said (R)-2-amino-1-phenylethanol derivative of the formula (V), R⁶, R⁷, R⁸ and R¹⁰ respectively represent a hydrogen atom, a C₁₋₄ alkyl group, a C₁₋₄ haloalkyl group, a C₁₋₄ alkoxy group, a nitro group or a halogen atom; and Z is a hydrogen atom or a protective group for a hydroxyl group.
 4. A process for producing an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative according to claim 1, wherein said (R)-2-amino-1-phenylethanol derivative of the formula (V), R⁹ is a C₁₋₄ haloalkyl group, a halogen atom or a nitro group; R⁶, R⁷, R⁸ and R¹⁰ are independently a hydrogen atom or a C₁₋₄ alkyl group; and Z is a hydrogen atom or a protective group for a hydroxyl group.
 5. A process for producing an (R,R)-1-phenyl-2- (2-phenyl-1-methylethyl)amino!ethanol derivative according to claim 1, wherein the reaction of the compound represented by the formula (V) and the compound represented by the formula (IV) is carried out in the presence of a dialkylamine. 